rs35594137
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs35594137(A;A) |
Make rs35594137(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 147773393 |
Gene | GJA5, LOC102723321 |
is a | snp |
is | mentioned by |
dbSNP | rs35594137 |
dbSNP (classic) | rs35594137 |
ClinGen | rs35594137 |
ebi | rs35594137 |
HLI | rs35594137 |
Exac | rs35594137 |
Gnomad | rs35594137 |
Varsome | rs35594137 |
LitVar | rs35594137 |
Map | rs35594137 |
PheGenI | rs35594137 |
Biobank | rs35594137 |
1000 genomes | rs35594137 |
hgdp | rs35594137 |
ensembl | rs35594137 |
geneview | rs35594137 |
scholar | rs35594137 |
rs35594137 | |
pharmgkb | rs35594137 |
gwascentral | rs35594137 |
openSNP | rs35594137 |
23andMe | rs35594137 |
SNPshot | rs35594137 |
SNPdbe | rs35594137 |
MSV3d | rs35594137 |
GWAS Ctlg | rs35594137 |
GMAF | 0.2218 |
Max Magnitude | 0 |
[PMID 21076161] A Common Connexin-40 Gene Promoter Variant Affects Connexin-40 Expression in Human Atria and Is Associated with Atrial Fibrillation
[PMID 25992486] Two polymorphisms in the Cx40 promoter are associated with hypertension and left ventricular hypertrophy preferentially in men
ClinVar | |
---|---|
Risk | rs35594137(A;A) |
Alt | rs35594137(A;A) |
Reference | Rs35594137(G;G) |
Significance | Probable-non-pathogenic |
Disease | Familial atrial fibrillation |
Variation | info |
Gene | GJA5 |
CLNDBN | Familial atrial fibrillation |
Reversed | 1 |
HGVS | NC_000001.10:g.147245497C>T |
CLNSRC | |
CLNACC | RCV000316019.1, |
[PMID 31270966] The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population.