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rs34978822

From SNPedia

Orientationplus
Make rs34978822(C;C)
Make rs34978822(C;G)
Make rs34978822(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63660246
GeneRTEL1, RTEL1-TNFRSF6B
is asnp
is mentioned by
dbSNPrs34978822
ebirs34978822
HLIrs34978822
Exacrs34978822
Varsomers34978822
Maprs34978822
PheGenIrs34978822
hapmaprs34978822
1000 genomesrs34978822
hgdprs34978822
ensemblrs34978822
gopubmedrs34978822
geneviewrs34978822
scholarrs34978822
googlers34978822
pharmgkbrs34978822
gwascentralrs34978822
openSNPrs34978822
23andMers34978822
23andMe allrs34978822
SNP Nexus

SNPshotrs34978822
SNPdbers34978822
MSV3drs34978822
GWAS Ctlgrs34978822
Max Magnitude

[PMID 27459707] Telomere structure and maintenance gene variants and risk of five cancer types.