rs146405172
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs146405172(A;A) |
Make rs146405172(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 99811603 |
Gene | ABCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs146405172 |
dbSNP (classic) | rs146405172 |
ClinGen | rs146405172 |
ebi | rs146405172 |
HLI | rs146405172 |
Exac | rs146405172 |
Gnomad | rs146405172 |
Varsome | rs146405172 |
LitVar | rs146405172 |
Map | rs146405172 |
PheGenI | rs146405172 |
Biobank | rs146405172 |
1000 genomes | rs146405172 |
hgdp | rs146405172 |
ensembl | rs146405172 |
geneview | rs146405172 |
scholar | rs146405172 |
rs146405172 | |
pharmgkb | rs146405172 |
gwascentral | rs146405172 |
openSNP | rs146405172 |
23andMe | rs146405172 |
SNPshot | rs146405172 |
SNPdbe | rs146405172 |
MSV3d | rs146405172 |
GWAS Ctlg | rs146405172 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146405172(A;A) |
Alt | rs146405172(A;A) |
Reference | Rs146405172(G;G) |
Significance | Pathogenic |
Disease | Dubin-Johnson syndrome |
Variation | info |
Gene | ABCC2 |
CLNDBN | Dubin-Johnson syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.101571360G>A |
CLNSRC | |
CLNACC | RCV000174845.1, |