rs10501920
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs10501920(C;G) |
Make rs10501920(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 99622442 |
Gene | CNTN5 |
is a | snp |
is | mentioned by |
dbSNP | rs10501920 |
dbSNP (classic) | rs10501920 |
ClinGen | rs10501920 |
ebi | rs10501920 |
HLI | rs10501920 |
Exac | rs10501920 |
Gnomad | rs10501920 |
Varsome | rs10501920 |
LitVar | rs10501920 |
Map | rs10501920 |
PheGenI | rs10501920 |
Biobank | rs10501920 |
1000 genomes | rs10501920 |
hgdp | rs10501920 |
ensembl | rs10501920 |
geneview | rs10501920 |
scholar | rs10501920 |
rs10501920 | |
pharmgkb | rs10501920 |
gwascentral | rs10501920 |
openSNP | rs10501920 |
23andMe | rs10501920 |
SNPshot | rs10501920 |
SNPdbe | rs10501920 |
MSV3d | rs10501920 |
GWAS Ctlg | rs10501920 |
GMAF | 0.1478 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs10501920 |
PubMedID | [PMID 17903304] |
Condition | Atrial fibrillation |
Gene | CNTN5 |
Risk Allele | |
pValue | 9.00E-006 |
OR | NA |
95% CI |