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rs11732231

From SNPedia

Orientationplus
Stabilizedplus
Make rs11732231(C;C)
Make rs11732231(C;G)
Make rs11732231(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position85762407
GeneARHGAP24
is asnp
is mentioned by
dbSNPrs11732231
ebirs11732231
HLIrs11732231
Exacrs11732231
Varsomers11732231
Maprs11732231
PheGenIrs11732231
hapmaprs11732231
1000 genomesrs11732231
hgdprs11732231
ensemblrs11732231
gopubmedrs11732231
geneviewrs11732231
scholarrs11732231
googlers11732231
pharmgkbrs11732231
gwascentralrs11732231
openSNPrs11732231
23andMers11732231
23andMe allrs11732231
SNP Nexus

SNPshotrs11732231
SNPdbers11732231
MSV3drs11732231
GWAS Ctlgrs11732231
GMAF0.3269
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23139255OA-icon.png]
Trait PR interval
Title Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts.
Risk Allele C
P-val 3E-9
Odds Ratio 2.28 [1.52-3.04] unit increase