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rs16970849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16970849(A;A)
Make rs16970849(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position78137827
GeneTMC8
is asnp
is mentioned by
dbSNPrs16970849
ebirs16970849
HLIrs16970849
Exacrs16970849
Varsomers16970849
Maprs16970849
PheGenIrs16970849
hapmaprs16970849
1000 genomesrs16970849
hgdprs16970849
ensemblrs16970849
gopubmedrs16970849
geneviewrs16970849
scholarrs16970849
googlers16970849
pharmgkbrs16970849
gwascentralrs16970849
openSNPrs16970849
23andMers16970849
23andMe allrs16970849
SNP Nexus

SNPshotrs16970849
SNPdbers16970849
MSV3drs16970849
GWAS Ctlgrs16970849
GMAF0.1598
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21387292OA-icon.png] Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility