rs398123133
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs398123133(-;-) |
Make rs398123133(-;A) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 77989827 |
Gene | ATP7A |
is a | snp |
is | mentioned by |
dbSNP | rs398123133 |
dbSNP (classic) | rs398123133 |
ClinGen | rs398123133 |
ebi | rs398123133 |
HLI | rs398123133 |
Exac | rs398123133 |
Gnomad | rs398123133 |
Varsome | rs398123133 |
LitVar | rs398123133 |
Map | rs398123133 |
PheGenI | rs398123133 |
Biobank | rs398123133 |
1000 genomes | rs398123133 |
hgdp | rs398123133 |
ensembl | rs398123133 |
geneview | rs398123133 |
scholar | rs398123133 |
rs398123133 | |
pharmgkb | rs398123133 |
gwascentral | rs398123133 |
openSNP | rs398123133 |
23andMe | rs398123133 |
SNPshot | rs398123133 |
SNPdbe | rs398123133 |
MSV3d | rs398123133 |
GWAS Ctlg | rs398123133 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398123133(-;-) |
Alt | rs398123133(-;-) |
Reference | Rs398123133(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP7A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.77245323delA |
CLNSRC | ClinVar |
CLNACC | RCV000078031.4, |