rs34937870
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs34937870(A;A) |
Make rs34937870(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 99842094 |
Gene | ABCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs34937870 |
dbSNP (classic) | rs34937870 |
ClinGen | rs34937870 |
ebi | rs34937870 |
HLI | rs34937870 |
Exac | rs34937870 |
Gnomad | rs34937870 |
Varsome | rs34937870 |
LitVar | rs34937870 |
Map | rs34937870 |
PheGenI | rs34937870 |
Biobank | rs34937870 |
1000 genomes | rs34937870 |
hgdp | rs34937870 |
ensembl | rs34937870 |
geneview | rs34937870 |
scholar | rs34937870 |
rs34937870 | |
pharmgkb | rs34937870 |
gwascentral | rs34937870 |
openSNP | rs34937870 |
23andMe | rs34937870 |
SNPshot | rs34937870 |
SNPdbe | rs34937870 |
MSV3d | rs34937870 |
GWAS Ctlg | rs34937870 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34937870(A;A) rs34937870(T;T) |
Alt | rs34937870(A;A) rs34937870(T;T) |
Reference | Rs34937870(G;G) |
Significance | Pathogenic |
Disease | Dubin-Johnson syndrome |
Variation | info |
Gene | ABCC2 |
CLNDBN | Dubin-Johnson syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.101601851G>A |
CLNSRC | |
CLNACC | RCV000190561.1, |