rs573535377
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs573535377(G;T) |
Make rs573535377(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 19 |
Position | 41981991 |
Gene | ATP1A3 |
is a | snp |
is | mentioned by |
dbSNP | rs573535377 |
dbSNP (classic) | rs573535377 |
ClinGen | rs573535377 |
ebi | rs573535377 |
HLI | rs573535377 |
Exac | rs573535377 |
Gnomad | rs573535377 |
Varsome | rs573535377 |
LitVar | rs573535377 |
Map | rs573535377 |
PheGenI | rs573535377 |
Biobank | rs573535377 |
1000 genomes | rs573535377 |
hgdp | rs573535377 |
ensembl | rs573535377 |
geneview | rs573535377 |
scholar | rs573535377 |
rs573535377 | |
pharmgkb | rs573535377 |
gwascentral | rs573535377 |
openSNP | rs573535377 |
23andMe | rs573535377 |
SNPshot | rs573535377 |
SNPdbe | rs573535377 |
MSV3d | rs573535377 |
GWAS Ctlg | rs573535377 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs573535377(T;T) |
Alt | rs573535377(T;T) |
Reference | Rs573535377(G;G) |
Significance | Pathogenic |
Disease | Dystonia 12 |
Variation | info |
Gene | ATP1A3 |
CLNDBN | Dystonia 12 |
Reversed | 0 |
HGVS | NC_000019.9:g.42486143G>T |
CLNSRC | ClinVar |
CLNACC | RCV000148336.1, |