rs186924074
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs186924074(A;G) |
Make rs186924074(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 13 |
Position | 51961861 |
Gene | ATP7B |
is a | snp |
is | mentioned by |
dbSNP | rs186924074 |
dbSNP (classic) | rs186924074 |
ClinGen | rs186924074 |
ebi | rs186924074 |
HLI | rs186924074 |
Exac | rs186924074 |
Gnomad | rs186924074 |
Varsome | rs186924074 |
LitVar | rs186924074 |
Map | rs186924074 |
PheGenI | rs186924074 |
Biobank | rs186924074 |
1000 genomes | rs186924074 |
hgdp | rs186924074 |
ensembl | rs186924074 |
geneview | rs186924074 |
scholar | rs186924074 |
rs186924074 | |
pharmgkb | rs186924074 |
gwascentral | rs186924074 |
openSNP | rs186924074 |
23andMe | rs186924074 |
SNPshot | rs186924074 |
SNPdbe | rs186924074 |
MSV3d | rs186924074 |
GWAS Ctlg | rs186924074 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs186924074(G;G) |
Alt | rs186924074(G;G) |
Reference | Rs186924074(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP7B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.52535997A>G |
CLNSRC | |
CLNACC | RCV000480322.1, |