rs886044573
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TT;TT) | 0 | common in clinvar |
Chromosome | 10 |
Position | 99834520 |
Gene | ABCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs886044573 |
dbSNP (classic) | rs886044573 |
ClinGen | rs886044573 |
ebi | rs886044573 |
HLI | rs886044573 |
Exac | rs886044573 |
Gnomad | rs886044573 |
Varsome | rs886044573 |
LitVar | rs886044573 |
Map | rs886044573 |
PheGenI | rs886044573 |
Biobank | rs886044573 |
1000 genomes | rs886044573 |
hgdp | rs886044573 |
ensembl | rs886044573 |
geneview | rs886044573 |
scholar | rs886044573 |
rs886044573 | |
pharmgkb | rs886044573 |
gwascentral | rs886044573 |
openSNP | rs886044573 |
23andMe | rs886044573 |
SNPshot | rs886044573 |
SNPdbe | rs886044573 |
MSV3d | rs886044573 |
GWAS Ctlg | rs886044573 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886044573(-;-) |
Alt | rs886044573(-;-) |
Reference | Rs886044573(TT;TT) |
Significance | Pathogenic |
Disease | Dubin-Johnson syndrome |
Variation | info |
Gene | ABCC2 |
CLNDBN | Dubin-Johnson syndrome |
Reversed | 0 |
HGVS | NC_000010.10:g.101594277_101594278delTT |
CLNSRC | |
CLNACC | RCV000366725.1, |