rs6666258
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6666258(C;C) |
Make rs6666258(C;G) |
Make rs6666258(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 154841792 |
Gene | KCNN3 |
is a | snp |
is | mentioned by |
dbSNP | rs6666258 |
dbSNP (classic) | rs6666258 |
ClinGen | rs6666258 |
ebi | rs6666258 |
HLI | rs6666258 |
Exac | rs6666258 |
Gnomad | rs6666258 |
Varsome | rs6666258 |
LitVar | rs6666258 |
Map | rs6666258 |
PheGenI | rs6666258 |
Biobank | rs6666258 |
1000 genomes | rs6666258 |
hgdp | rs6666258 |
ensembl | rs6666258 |
geneview | rs6666258 |
scholar | rs6666258 |
rs6666258 | |
pharmgkb | rs6666258 |
gwascentral | rs6666258 |
openSNP | rs6666258 |
23andMe | rs6666258 |
SNPshot | rs6666258 |
SNPdbe | rs6666258 |
MSV3d | rs6666258 |
GWAS Ctlg | rs6666258 |
GMAF | 0.2479 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22544366![]() |
Trait | |
Title | Meta-analysis identifies six new susceptibility loci for atrial fibrillation. |
Risk Allele | C |
P-val | 2E-14 |
Odds Ratio | 1.1800 None |
[PMID 27179719] Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation.
[PMID 29624624] Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.