rs869025341
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs869025341(A;A) |
Make rs869025341(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 160124371 |
Gene | ATP1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs869025341 |
dbSNP (classic) | rs869025341 |
ClinGen | rs869025341 |
ebi | rs869025341 |
HLI | rs869025341 |
Exac | rs869025341 |
Gnomad | rs869025341 |
Varsome | rs869025341 |
LitVar | rs869025341 |
Map | rs869025341 |
PheGenI | rs869025341 |
Biobank | rs869025341 |
1000 genomes | rs869025341 |
hgdp | rs869025341 |
ensembl | rs869025341 |
geneview | rs869025341 |
scholar | rs869025341 |
rs869025341 | |
pharmgkb | rs869025341 |
gwascentral | rs869025341 |
openSNP | rs869025341 |
23andMe | rs869025341 |
SNPshot | rs869025341 |
SNPdbe | rs869025341 |
MSV3d | rs869025341 |
GWAS Ctlg | rs869025341 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025341(A;A) |
Alt | rs869025341(A;A) |
Reference | Rs869025341(G;G) |
Significance | Pathogenic |
Disease | Familial hemiplegic migraine type 2 |
Variation | info |
Gene | ATP1A2 |
CLNDBN | Familial hemiplegic migraine type 2 |
Reversed | 0 |
HGVS | NC_000001.10:g.160094161G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000207519.1, |