G RTEL1 | |||
Description: regulator of telomere elongation helicase 1 Associations 126 Studies 98 |
G RTEL1-TNFRSF6B | |||
Description: RTEL1-TNFRSF6B readthrough (NMD candidate) Associations 144 Studies 115 |
P Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. | |||
Delgado DA et al. 2017 J Med Genet PMID:29151059 Associations 7 Studies 1 |
P Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. | |||
Wrensch M et al. 2009 Nat Genet PMID:19578366 Associations 3 Studies 1 |
V rs6010620 | |||
Location: 20:63678486 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 10 Studies 10 |
V rs6011002 | |||
Location: 20:63666449 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs2297441 | |||
Location: 20:63696229 Cytogenetic region:20q13.33 Most severe consequence: 3 prime utr variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs4809324 | |||
Location: 20:63686867 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs2236507 | |||
Location: 20:63691653 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs6062302 | |||
Location: 20:63689615 Cytogenetic region:20q13.33 Most severe consequence: Synonymous variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 4 Studies 4 |
V rs4809219 | |||
Location: 20:63671762 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs3787096 | |||
Location: 20:63676805 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs2297440 | |||
Location: 20:63680946 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 11 Studies 7 |
V rs6011033 | |||
Location: 20:63691346 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 9 Studies 9 |
V rs2297439 | |||
Location: 20:63679775 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs8114049 | |||
Location: 20:63679453 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs6089956 | |||
Location: 20:63677011 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs35640778 | |||
Location: 20:63689775 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 9 Studies 9 |
V rs3208007 | |||
Location: 20:63690935 Cytogenetic region:20q13.33 Most severe consequence: Synonymous variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 3 Studies 3 |
V rs2738783 | |||
Location: 20:63677259 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 4 Studies 4 |
V rs41309367 | |||
Location: 20:63678201 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs80132799 | |||
Location: 20:63691543 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs7361098 | |||
Location: 20:63681402 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs2738784 | |||
Location: 20:63679219 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs3787100 | |||
Location: 20:63675057 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs3787089 | |||
Location: 20:63685277 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs41308092 | |||
Location: 20:63693038 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs143190905 | |||
Location: 20:63660414 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs34978822 | |||
Location: 20:63660246 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 5 Studies 5 |
V rs6062486 | |||
Location: 20:63671186 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs139221232 | |||
Location: 20:63693256 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs3787099 | |||
Location: 20:63676164 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs2297433 | |||
Location: 20:63662107 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs41308088 | |||
Location: 20:63661765 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 6 Studies 6 |
V rs3838004 | |||
Location: 20:63676910 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs3848669 | |||
Location: 20:63669458 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs6122140 | |||
Location: 20:63664776 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs2738782 | |||
Location: 20:63677217 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs79981941 | |||
Location: 20:63676585 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs181080831 | |||
Location: 20:63695521 Cytogenetic region:20q13.33 Most severe consequence: Synonymous variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs75031349 | |||
Location: 20:63682701 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs6062295 | |||
Location: 20:63659821 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs61753459 | |||
Location: 20:63689836 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs77552606 | |||
Location: 20:63679776 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs1056990 | |||
Location: 20:63695846 Cytogenetic region:20q13.33 Most severe consequence: Synonymous variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs79834248 | |||
Location: 20:63670906 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs6011023 | |||
Location: 20:63675195 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs11696198 | |||
Location: 20:63667051 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs34412639 | |||
Location: 20:63691580 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs35902944 | |||
Location: 20:63677042 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs187013287 | |||
Location: 20:63667021 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs190887884 | |||
Location: 20:63690937 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs41309931 | |||
Location: 20:63695226 Cytogenetic region:20q13.33 Most severe consequence: Splice donor 5th base variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs41308090 | |||
Location: 20:63693063 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs62207047 | |||
Location: 20:63679610 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs112914646 | |||
Location: 20:63679469 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs6089763 | |||
Location: 20:63677001 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs34538116 | |||
Location: 20:63677077 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs6011026 | |||
Location: 20:63677133 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): RTEL1,RTEL1-TNFRSF6B Associations 1 Studies 1 |
V rs909341 | |||
Location: 20:63697389 Cytogenetic region:20q13.33 Most severe consequence: Missense variant Mapped gene(s): TNFRSF6B,RTEL1-TNFRSF6B Associations 2 Studies 2 |
V rs6062496 | |||
Location: 20:63697746 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): TNFRSF6B,RTEL1-TNFRSF6B Associations 9 Studies 9 |
V rs2738787 | |||
Location: 20:63697022 Cytogenetic region:20q13.33 Most severe consequence: Synonymous variant Mapped gene(s): TNFRSF6B,RTEL1-TNFRSF6B Associations 6 Studies 6 |
V rs74748720 | |||
Location: 20:63697813 Cytogenetic region:20q13.33 Most severe consequence: Intron variant Mapped gene(s): TNFRSF6B,RTEL1-TNFRSF6B Associations 1 Studies 1 |