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rs11708896

From SNPedia

Orientationplus
Stabilizedplus
Make rs11708896(A;A)
Make rs11708896(A;G)
Make rs11708896(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position7795937
is asnp
is mentioned by
dbSNPrs11708896
ebirs11708896
HLIrs11708896
Exacrs11708896
Varsomers11708896
Maprs11708896
PheGenIrs11708896
hapmaprs11708896
1000 genomesrs11708896
hgdprs11708896
ensemblrs11708896
gopubmedrs11708896
geneviewrs11708896
scholarrs11708896
googlers11708896
pharmgkbrs11708896
gwascentralrs11708896
openSNPrs11708896
23andMers11708896
23andMe allrs11708896
SNP Nexus

SNPshotrs11708896
SNPdbers11708896
MSV3drs11708896
GWAS Ctlgrs11708896
GMAF0.3228
Max Magnitude
GWAS snp
PMID [PMID 20062060OA-icon.png]
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