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rs6089953

From SNPedia

Orientationplus
Stabilizedplus
Make rs6089953(A;A)
Make rs6089953(A;G)
Make rs6089953(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position63659655
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs6089953
dbSNP (classic)rs6089953
ClinGenrs6089953
ebirs6089953
HLIrs6089953
Exacrs6089953
Gnomadrs6089953
Varsomers6089953
LitVarrs6089953
Maprs6089953
PheGenIrs6089953
Biobankrs6089953
1000 genomesrs6089953
hgdprs6089953
ensemblrs6089953
geneviewrs6089953
scholarrs6089953
googlers6089953
pharmgkbrs6089953
gwascentralrs6089953
openSNPrs6089953
23andMers6089953
SNPshotrs6089953
SNPdbers6089953
MSV3drs6089953
GWAS Ctlgrs6089953
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 26014354] CCDC26, CDKN2BAS, RTEL1 and TERT Polymorphisms in pediatric brain tumor susceptibility


[PMID 30462709OA-icon.png] Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population.