rs11708896
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11708896(A;A) |
Make rs11708896(A;G) |
Make rs11708896(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 7795937 |
is a | snp |
is | mentioned by |
dbSNP | rs11708896 |
dbSNP (classic) | rs11708896 |
ClinGen | rs11708896 |
ebi | rs11708896 |
HLI | rs11708896 |
Exac | rs11708896 |
Gnomad | rs11708896 |
Varsome | rs11708896 |
LitVar | rs11708896 |
Map | rs11708896 |
PheGenI | rs11708896 |
Biobank | rs11708896 |
1000 genomes | rs11708896 |
hgdp | rs11708896 |
ensembl | rs11708896 |
geneview | rs11708896 |
scholar | rs11708896 |
rs11708896 | |
pharmgkb | rs11708896 |
gwascentral | rs11708896 |
openSNP | rs11708896 |
23andMe | rs11708896 |
SNPshot | rs11708896 |
SNPdbe | rs11708896 |
MSV3d | rs11708896 |
GWAS Ctlg | rs11708896 |
GMAF | 0.3228 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 20062060![]() |
Trait | PR interval |
Title | Genome-wide association study of PR interval |
Risk Allele | C |
P-val | 6E-26 |
Odds Ratio | 3.04 [2.47-3.61] ms increase |