G RYR2 | |||
Description: ryanodine receptor 2 Associations 113 Studies 77 |
V rs7529251 | |||
Location: 1:237435116 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs1478912 | |||
Location: 1:237457939 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs268786 | |||
Location: 1:237192685 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7554607 | |||
Location: 1:237103303 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6683225 | |||
Location: 1:237186438 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2819742 | |||
Location: 1:237826822 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2819770 | |||
Location: 1:237747704 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs876793 | |||
Location: 1:237688783 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 5 Studies 5 |
V rs10925507 | |||
Location: 1:237749981 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2685295 | |||
Location: 1:237735135 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs143294628 | |||
Location: 1:237653650 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2490361 | |||
Location: 1:237163674 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6677658 | |||
Location: 1:237396237 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2797436 | |||
Location: 1:237700418 Cytogenetic region:1q43 Most severe consequence: Synonymous variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs3820572 | |||
Location: 1:237602357 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs3766889 | |||
Location: 1:237778481 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 2 |
V rs10925358 | |||
Location: 1:237287133 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7528353 | |||
Location: 1:237425165 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs192540202 | |||
Location: 1:237348241 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs4659805 | |||
Location: 1:237696455 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 2 |
V rs1891248 | |||
Location: 1:237829735 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs34967813 | |||
Location: 1:237678090 Cytogenetic region:1q43 Most severe consequence: Missense variant Mapped gene(s): RYR2 Associations 9 Studies 9 |
V rs813173 | |||
Location: 1:237811420 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7535911 | |||
Location: 1:237327441 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs200918659 | |||
Location: 1:237402409 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs34729156 | |||
Location: 1:237571716 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 2 |
V rs3766884 | |||
Location: 1:237712988 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2485558 | |||
Location: 1:237115225 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 5 Studies 5 |
V rs12122723 | |||
Location: 1:237427889 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2255179 | |||
Location: 1:237580596 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 1 |
V rs2618720 | |||
Location: 1:237566218 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 1 |
V rs10495397 | |||
Location: 1:237495847 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs140263733 | |||
Location: 1:237395119 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10802610 | |||
Location: 1:237406417 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12041884 | |||
Location: 1:237402409 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs78072807 | |||
Location: 1:237519633 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs578741 | |||
Location: 1:237621917 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 2 |
V rs918241 | |||
Location: 1:237256786 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7520927 | |||
Location: 1:237583515 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs3753629 | |||
Location: 1:237637472 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2790348 | |||
Location: 1:237803193 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2997971 | |||
Location: 1:237438808 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2618703 | |||
Location: 1:237527984 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10802599 | |||
Location: 1:237307101 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs961120 | |||
Location: 1:237259907 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2111735 | |||
Location: 1:237256500 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs112387072 | |||
Location: 1:237591663 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 2 Studies 2 |
V rs636167 | |||
Location: 1:237238965 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2543037 | |||
Location: 1:237338122 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10802595 | |||
Location: 1:237256994 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs2485572 | |||
Location: 1:237125525 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs75310728 | |||
Location: 1:237333203 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10925333 | |||
Location: 1:237152803 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10925406 | |||
Location: 1:237398497 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs112406313 | |||
Location: 1:237529846 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs114119896 | |||
Location: 1:237397702 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs538680895 | |||
Location: 1:237803501 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs958170362 | |||
Location: 1:237709337 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs1832340 | |||
Location: 1:237236567 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs61832415 | |||
Location: 1:237216967 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs11587851 | |||
Location: 1:237237755 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs1362844 | |||
Location: 1:237239492 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12408892 | |||
Location: 1:237237138 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs55924146 | |||
Location: 1:237238700 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10925347 | |||
Location: 1:237236848 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs11584450 | |||
Location: 1:237238147 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs10802591 | |||
Location: 1:237220093 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7541818 | |||
Location: 1:237220594 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6665340 | |||
Location: 1:237221019 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6661229 | |||
Location: 1:237219389 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs72764084 | |||
Location: 1:237238067 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs72764083 | |||
Location: 1:237238060 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12078693 | |||
Location: 1:237230424 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6683160 | |||
Location: 1:237227432 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs11801278 | |||
Location: 1:237230784 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs7541924 | |||
Location: 1:237220697 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12407646 | |||
Location: 1:237228579 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs6703530 | |||
Location: 1:237217888 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12137834 | |||
Location: 1:237241309 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs12032174 | |||
Location: 1:237692868 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 3 Studies 3 |
V rs10802580 | |||
Location: 1:237031622 Cytogenetic region:1q43 Most severe consequence: Regulatory region variant Mapped gene(s): RYR2,MT1HL1 Associations 5 Studies 5 |
V rs10675131 (rs35534155) | |||
Location: 1:237044644 Cytogenetic region:1q43 Most severe consequence: Intron variant Mapped gene(s): RYR2 Associations 1 Studies 1 |
V rs813762 | |||
Location: 1:237848353 Cytogenetic region:1q43 Most severe consequence: Intergenic variant Mapped gene(s): RYR2,ZP4 Associations 1 Studies 1 |
V rs34521262 | |||
Location: 1:237846589 Cytogenetic region:1q43 Most severe consequence: Intergenic variant Mapped gene(s): RYR2,ZP4 Associations 1 Studies 1 |