rs11552588
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs11552588(A;G) |
Make rs11552588(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 147773279 |
Gene | GJA5, LOC102723321 |
is a | snp |
is | mentioned by |
dbSNP | rs11552588 |
dbSNP (classic) | rs11552588 |
ClinGen | rs11552588 |
ebi | rs11552588 |
HLI | rs11552588 |
Exac | rs11552588 |
Gnomad | rs11552588 |
Varsome | rs11552588 |
LitVar | rs11552588 |
Map | rs11552588 |
PheGenI | rs11552588 |
Biobank | rs11552588 |
1000 genomes | rs11552588 |
hgdp | rs11552588 |
ensembl | rs11552588 |
geneview | rs11552588 |
scholar | rs11552588 |
rs11552588 | |
pharmgkb | rs11552588 |
gwascentral | rs11552588 |
openSNP | rs11552588 |
23andMe | rs11552588 |
SNPshot | rs11552588 |
SNPdbe | rs11552588 |
MSV3d | rs11552588 |
GWAS Ctlg | rs11552588 |
Max Magnitude | 0 |
[PMID 25992486] Two polymorphisms in the Cx40 promoter are associated with hypertension and left ventricular hypertrophy preferentially in men
ClinVar | |
---|---|
Risk | rs11552588(G;G) |
Alt | rs11552588(G;G) |
Reference | Rs11552588(A;A) |
Significance | Probable-non-pathogenic |
Disease | Familial atrial fibrillation |
Variation | info |
Gene | GJA5 |
CLNDBN | Familial atrial fibrillation |
Reversed | 1 |
HGVS | NC_000001.10:g.147245383T>C |
CLNSRC | |
CLNACC | RCV000330907.1, |