rs3815676
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 |
Make rs3815676(A;G) |
Make rs3815676(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 169013869 |
Gene | ABCB11 |
is a | snp |
is | mentioned by |
dbSNP | rs3815676 |
dbSNP (classic) | rs3815676 |
ClinGen | rs3815676 |
ebi | rs3815676 |
HLI | rs3815676 |
Exac | rs3815676 |
Gnomad | rs3815676 |
Varsome | rs3815676 |
LitVar | rs3815676 |
Map | rs3815676 |
PheGenI | rs3815676 |
Biobank | rs3815676 |
1000 genomes | rs3815676 |
hgdp | rs3815676 |
ensembl | rs3815676 |
geneview | rs3815676 |
scholar | rs3815676 |
rs3815676 | |
pharmgkb | rs3815676 |
gwascentral | rs3815676 |
openSNP | rs3815676 |
23andMe | rs3815676 |
SNPshot | rs3815676 |
SNPdbe | rs3815676 |
MSV3d | rs3815676 |
GWAS Ctlg | rs3815676 |
GMAF | 0.04775 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24366234] A Comprehensive Analysis of Common Genetic Variation Around Six Candidate Loci for Intrahepatic Cholestasis of Pregnancy