rs201977531
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs201977531(A;G) |
Make rs201977531(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 160134547 |
Gene | ATP1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs201977531 |
dbSNP (classic) | rs201977531 |
ClinGen | rs201977531 |
ebi | rs201977531 |
HLI | rs201977531 |
Exac | rs201977531 |
Gnomad | rs201977531 |
Varsome | rs201977531 |
LitVar | rs201977531 |
Map | rs201977531 |
PheGenI | rs201977531 |
Biobank | rs201977531 |
1000 genomes | rs201977531 |
hgdp | rs201977531 |
ensembl | rs201977531 |
geneview | rs201977531 |
scholar | rs201977531 |
rs201977531 | |
pharmgkb | rs201977531 |
gwascentral | rs201977531 |
openSNP | rs201977531 |
23andMe | rs201977531 |
SNPshot | rs201977531 |
SNPdbe | rs201977531 |
MSV3d | rs201977531 |
GWAS Ctlg | rs201977531 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201977531(G;G) |
Alt | rs201977531(G;G) |
Reference | Rs201977531(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP1A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.160104337A>G |
CLNSRC | |
CLNACC | RCV000186795.2, |