rs16970849
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs16970849(A;A) |
Make rs16970849(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 78137827 |
Gene | TMC8 |
is a | snp |
is | mentioned by |
dbSNP | rs16970849 |
dbSNP (classic) | rs16970849 |
ClinGen | rs16970849 |
ebi | rs16970849 |
HLI | rs16970849 |
Exac | rs16970849 |
Gnomad | rs16970849 |
Varsome | rs16970849 |
LitVar | rs16970849 |
Map | rs16970849 |
PheGenI | rs16970849 |
Biobank | rs16970849 |
1000 genomes | rs16970849 |
hgdp | rs16970849 |
ensembl | rs16970849 |
geneview | rs16970849 |
scholar | rs16970849 |
rs16970849 | |
pharmgkb | rs16970849 |
gwascentral | rs16970849 |
openSNP | rs16970849 |
23andMe | rs16970849 |
SNPshot | rs16970849 |
SNPdbe | rs16970849 |
MSV3d | rs16970849 |
GWAS Ctlg | rs16970849 |
GMAF | 0.1598 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21387292] Contribution of TMC6 and TMC8 (EVER1 and EVER2) variants to cervical cancer susceptibility