rs755287627
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs755287627(A;G) |
Make rs755287627(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 113353494 |
Gene | ANK2 |
is a | snp |
is | mentioned by |
dbSNP | rs755287627 |
dbSNP (classic) | rs755287627 |
ClinGen | rs755287627 |
ebi | rs755287627 |
HLI | rs755287627 |
Exac | rs755287627 |
Gnomad | rs755287627 |
Varsome | rs755287627 |
LitVar | rs755287627 |
Map | rs755287627 |
PheGenI | rs755287627 |
Biobank | rs755287627 |
1000 genomes | rs755287627 |
hgdp | rs755287627 |
ensembl | rs755287627 |
geneview | rs755287627 |
scholar | rs755287627 |
rs755287627 | |
pharmgkb | rs755287627 |
gwascentral | rs755287627 |
openSNP | rs755287627 |
23andMe | rs755287627 |
SNPshot | rs755287627 |
SNPdbe | rs755287627 |
MSV3d | rs755287627 |
GWAS Ctlg | rs755287627 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755287627(G;G) |
Alt | rs755287627(G;G) |
Reference | Rs755287627(A;A) |
Significance | Probable-Pathogenic |
Disease | Long QT syndrome |
Variation | info |
Gene | ANK2 |
CLNDBN | Long QT syndrome |
Reversed | 0 |
HGVS | NC_000004.11:g.114274650A>G |
CLNSRC | |
CLNACC | RCV000190219.1, |