rs71581941
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs71581941(C;T) |
Make rs71581941(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 21222355 |
Gene | SLCO1B1 |
is a | snp |
is | mentioned by |
dbSNP | rs71581941 |
dbSNP (classic) | rs71581941 |
ClinGen | rs71581941 |
ebi | rs71581941 |
HLI | rs71581941 |
Exac | rs71581941 |
Gnomad | rs71581941 |
Varsome | rs71581941 |
LitVar | rs71581941 |
Map | rs71581941 |
PheGenI | rs71581941 |
Biobank | rs71581941 |
1000 genomes | rs71581941 |
hgdp | rs71581941 |
ensembl | rs71581941 |
geneview | rs71581941 |
scholar | rs71581941 |
rs71581941 | |
pharmgkb | rs71581941 |
gwascentral | rs71581941 |
openSNP | rs71581941 |
23andMe | rs71581941 |
SNPshot | rs71581941 |
SNPdbe | rs71581941 |
MSV3d | rs71581941 |
GWAS Ctlg | rs71581941 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs71581941(A;A) rs71581941(T;T) |
Alt | rs71581941(A;A) rs71581941(T;T) |
Reference | Rs71581941(C;C) |
Significance | Pathogenic |
Disease | Rotor syndrome |
Variation | info |
Gene | SLCO1B1 |
CLNDBN | Rotor syndrome |
Reversed | 0 |
HGVS | NC_000012.11:g.21375289C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000023390.2, |