rs118109635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs118109635(A;A) |
Make rs118109635(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 168944621 |
Gene | ABCB11 |
is a | snp |
is | mentioned by |
dbSNP | rs118109635 |
dbSNP (classic) | rs118109635 |
ClinGen | rs118109635 |
ebi | rs118109635 |
HLI | rs118109635 |
Exac | rs118109635 |
Gnomad | rs118109635 |
Varsome | rs118109635 |
LitVar | rs118109635 |
Map | rs118109635 |
PheGenI | rs118109635 |
Biobank | rs118109635 |
1000 genomes | rs118109635 |
hgdp | rs118109635 |
ensembl | rs118109635 |
geneview | rs118109635 |
scholar | rs118109635 |
rs118109635 | |
pharmgkb | rs118109635 |
gwascentral | rs118109635 |
openSNP | rs118109635 |
23andMe | rs118109635 |
SNPshot | rs118109635 |
SNPdbe | rs118109635 |
MSV3d | rs118109635 |
GWAS Ctlg | rs118109635 |
Max Magnitude | 0 |
[PMID 25323205] Variations of ABCB4 and ABCB11 genes are associated with primary intrahepatic stones
ClinVar | |
---|---|
Risk | rs118109635(A;A) |
Alt | rs118109635(A;A) |
Reference | Rs118109635(G;G) |
Significance | Probable-non-pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | ABCB11 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000002.11:g.169801131G>A |
CLNSRC | |
CLNACC | RCV000224014.1, RCV000267628.1, |