rs67273048
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs67273048(A;A) |
Make rs67273048(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 78021030 |
Gene | ATP7A |
is a | snp |
is | mentioned by |
dbSNP | rs67273048 |
dbSNP (classic) | rs67273048 |
ClinGen | rs67273048 |
ebi | rs67273048 |
HLI | rs67273048 |
Exac | rs67273048 |
Gnomad | rs67273048 |
Varsome | rs67273048 |
LitVar | rs67273048 |
Map | rs67273048 |
PheGenI | rs67273048 |
Biobank | rs67273048 |
1000 genomes | rs67273048 |
hgdp | rs67273048 |
ensembl | rs67273048 |
geneview | rs67273048 |
scholar | rs67273048 |
rs67273048 | |
pharmgkb | rs67273048 |
gwascentral | rs67273048 |
openSNP | rs67273048 |
23andMe | rs67273048 |
SNPshot | rs67273048 |
SNPdbe | rs67273048 |
MSV3d | rs67273048 |
GWAS Ctlg | rs67273048 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs67273048(A;A) |
Alt | rs67273048(A;A) |
Reference | Rs67273048(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP7A |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.77276527G>A |
CLNSRC | |
CLNACC | RCV000420383.1, |