rs886042519
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Chromosome | 13 |
Position | 51939086 |
Gene | ATP7B |
is a | snp |
is | mentioned by |
dbSNP | rs886042519 |
dbSNP (classic) | rs886042519 |
ClinGen | rs886042519 |
ebi | rs886042519 |
HLI | rs886042519 |
Exac | rs886042519 |
Gnomad | rs886042519 |
Varsome | rs886042519 |
LitVar | rs886042519 |
Map | rs886042519 |
PheGenI | rs886042519 |
Biobank | rs886042519 |
1000 genomes | rs886042519 |
hgdp | rs886042519 |
ensembl | rs886042519 |
geneview | rs886042519 |
scholar | rs886042519 |
rs886042519 | |
pharmgkb | rs886042519 |
gwascentral | rs886042519 |
openSNP | rs886042519 |
23andMe | rs886042519 |
SNPshot | rs886042519 |
SNPdbe | rs886042519 |
MSV3d | rs886042519 |
GWAS Ctlg | rs886042519 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886042519(-;-) |
Alt | rs886042519(-;-) |
Reference | Rs886042519(C;C) |
Significance | Other |
Disease | Wilson disease |
Variation | info |
Gene | ATP7B |
CLNDBN | Wilson disease |
Reversed | 0 |
HGVS | NC_000013.10:g.52513222delC |
CLNSRC | |
CLNACC | RCV000333158.1, |