rs12302655
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs12302655(A;A) |
Make rs12302655(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 112936701 |
Gene | OAS3 |
is a | snp |
is | mentioned by |
dbSNP | rs12302655 |
dbSNP (classic) | rs12302655 |
ClinGen | rs12302655 |
ebi | rs12302655 |
HLI | rs12302655 |
Exac | rs12302655 |
Gnomad | rs12302655 |
Varsome | rs12302655 |
LitVar | rs12302655 |
Map | rs12302655 |
PheGenI | rs12302655 |
Biobank | rs12302655 |
1000 genomes | rs12302655 |
hgdp | rs12302655 |
ensembl | rs12302655 |
geneview | rs12302655 |
scholar | rs12302655 |
rs12302655 | |
pharmgkb | rs12302655 |
gwascentral | rs12302655 |
openSNP | rs12302655 |
23andMe | rs12302655 |
SNPshot | rs12302655 |
SNPdbe | rs12302655 |
MSV3d | rs12302655 |
GWAS Ctlg | rs12302655 |
GMAF | 0.09275 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 20084279] Common Genetic Variants and Risk for HPV Persistence and Progression to Cervical Cancer