G GRIN2A | |||
Description: glutamate ionotropic receptor NMDA type subunit 2A Associations 115 Studies 91 |
P Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. | |||
Hamza TH et al. 2011 PLoS Genet PMID:21876681 Associations 0 Studies 1 |
P A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection. | |||
Liu L et al. 2011 Viral Immunol PMID:22004137 Associations 1 Studies 1 |
V rs11866328 | |||
Location: 16:9768699 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs8058295 | |||
Location: 16:9817529 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1463132 | |||
Location: 16:10089230 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7203315 | |||
Location: 16:10094203 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs9922678 | |||
Location: 16:9852462 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 8 Studies 7 |
V rs6497540 | |||
Location: 16:9841209 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs3104705 | |||
Location: 16:9975433 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs3104707 | |||
Location: 16:9977301 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7191183 | |||
Location: 16:9806200 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 3 Studies 3 |
V rs140019346 | |||
Location: 16:9912050 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7206296 | |||
Location: 16:10053621 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs72774059 | |||
Location: 16:10007295 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs837705 | |||
Location: 16:10019519 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1420044 | |||
Location: 16:9820276 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs62035769 | |||
Location: 16:10122080 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs16966656 | |||
Location: 16:9898362 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1448258 | |||
Location: 16:10057500 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72776049 | |||
Location: 16:10127597 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1097784 | |||
Location: 16:10155559 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs35016816 | |||
Location: 16:10172258 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs193201466 | |||
Location: 16:9903074 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs17800861 | |||
Location: 16:9859815 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs12926704 | |||
Location: 16:10147597 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 4 Studies 4 |
V rs4780790 | |||
Location: 16:10087779 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs11074547 | |||
Location: 16:10043032 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs7192140 | |||
Location: 16:10079891 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 3 Studies 3 |
V rs4782271 | |||
Location: 16:10125560 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs2352744 | |||
Location: 16:10079196 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs11647445 | |||
Location: 16:9833109 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 4 Studies 4 |
V rs117304774 | |||
Location: 16:10057377 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs41356645 | |||
Location: 16:9852062 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1868289 | |||
Location: 16:10121956 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs4782108 | |||
Location: 16:9963734 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1875207 | |||
Location: 16:9965134 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72774191 | |||
Location: 16:10098624 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs11648559 | |||
Location: 16:9780842 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs9926049 | |||
Location: 16:9846103 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs60920123 | |||
Location: 16:10040780 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs12924396 | |||
Location: 16:9976428 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7199910 | |||
Location: 16:9832491 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs11074604 | |||
Location: 16:10131878 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7191999 | |||
Location: 16:9806627 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs7204266 | |||
Location: 16:9874646 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs12928694 | |||
Location: 16:9973686 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1103127 | |||
Location: 16:10140907 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs4780865 | |||
Location: 16:10176810 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs9674103 | |||
Location: 16:9815266 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1868285 | |||
Location: 16:10028600 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs8044064 | |||
Location: 16:10069876 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72772387 | |||
Location: 16:10059734 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs12932206 | |||
Location: 16:9972164 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs1104474 | |||
Location: 16:10174386 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7206714 | |||
Location: 16:10084138 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs2352743 | |||
Location: 16:10078911 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs12932099 | |||
Location: 16:10109624 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs6497676 | |||
Location: 16:10086366 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7189786 | |||
Location: 16:10111321 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7201930 | |||
Location: 16:9864798 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs2442098 | |||
Location: 16:10136362 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs13337187 | |||
Location: 16:10116448 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs12597701 | |||
Location: 16:9993071 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72772172 | |||
Location: 16:9982513 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 2 Studies 2 |
V rs28550823 | |||
Location: 16:10122386 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7190960 | |||
Location: 16:10043242 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72774188 | |||
Location: 16:10097366 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs8060239 | |||
Location: 16:10018451 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs4782268 | |||
Location: 16:10124917 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7190785 | |||
Location: 16:9779608 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs72772372 | |||
Location: 16:10050128 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs12934281 | |||
Location: 16:9814519 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs4782266 | |||
Location: 16:10124133 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs7204513 | |||
Location: 16:10123049 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A Associations 1 Studies 1 |
V rs6497441 | |||
Location: 16:9735991 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,LINC02177 Associations 1 Studies 1 |
V rs1833170 | |||
Location: 16:9728154 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,LINC02177 Associations 1 Studies 1 |
V rs117468730 | |||
Location: 16:10111610 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A,IMPDH1P11 Associations 2 Studies 2 |
V rs139215580 | |||
Location: 16:10205465 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs8046217 | |||
Location: 16:10195005 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs188650377 | |||
Location: 16:10192780 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs11074660 | |||
Location: 16:10214609 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs193149952 | |||
Location: 16:10192190 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs11641504 | |||
Location: 16:10111967 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A,IMPDH1P11 Associations 1 Studies 1 |
V rs11074658 | |||
Location: 16:10214478 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs1815981 | |||
Location: 16:9716066 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,LINC02177 Associations 1 Studies 1 |
V rs7200416 | |||
Location: 16:10206419 Cytogenetic region:16p13.2 Most severe consequence: Regulatory region variant Mapped gene(s): GRIN2A,RN7SL493P Associations 1 Studies 1 |
V rs11646975 | |||
Location: 16:9682871 Cytogenetic region:16p13.2 Most severe consequence: Intergenic variant Mapped gene(s): GRIN2A,LINC02177 Associations 1 Studies 1 |
V rs11866570 | |||
Location: 16:10112318 Cytogenetic region:16p13.2 Most severe consequence: Intron variant Mapped gene(s): GRIN2A,IMPDH1P11 Associations 1 Studies 1 |