rs755310507
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs755310507(A;A) |
Make rs755310507(A;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 160136307 |
Gene | ATP1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs755310507 |
dbSNP (classic) | rs755310507 |
ClinGen | rs755310507 |
ebi | rs755310507 |
HLI | rs755310507 |
Exac | rs755310507 |
Gnomad | rs755310507 |
Varsome | rs755310507 |
LitVar | rs755310507 |
Map | rs755310507 |
PheGenI | rs755310507 |
Biobank | rs755310507 |
1000 genomes | rs755310507 |
hgdp | rs755310507 |
ensembl | rs755310507 |
geneview | rs755310507 |
scholar | rs755310507 |
rs755310507 | |
pharmgkb | rs755310507 |
gwascentral | rs755310507 |
openSNP | rs755310507 |
23andMe | rs755310507 |
SNPshot | rs755310507 |
SNPdbe | rs755310507 |
MSV3d | rs755310507 |
GWAS Ctlg | rs755310507 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755310507(A;A) rs755310507(T;T) |
Alt | rs755310507(A;A) rs755310507(T;T) |
Reference | Rs755310507(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP1A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.160106097C>T |
CLNSRC | |
CLNACC | RCV000256148.1, |