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rs75316749

From SNPedia

Orientationplus
Make rs75316749(A;A)
Make rs75316749(A;G)
Make rs75316749(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position169043635
is asnp
is mentioned by
dbSNPrs75316749
ebirs75316749
HLIrs75316749
Exacrs75316749
Varsomers75316749
Maprs75316749
PheGenIrs75316749
hapmaprs75316749
1000 genomesrs75316749
hgdprs75316749
ensemblrs75316749
gopubmedrs75316749
geneviewrs75316749
scholarrs75316749
googlers75316749
pharmgkbrs75316749
gwascentralrs75316749
openSNPrs75316749
23andMers75316749
23andMe allrs75316749
SNP Nexus

SNPshotrs75316749
SNPdbers75316749
MSV3drs75316749
GWAS Ctlgrs75316749
Max Magnitude

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