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rs7692808

From SNPedia

Orientationplus
Stabilizedplus
Make rs7692808(A;A)
Make rs7692808(A;G)
Make rs7692808(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position85719996
GeneARHGAP24
is asnp
is mentioned by
dbSNPrs7692808
dbSNP (classic)rs7692808
ClinGenrs7692808
ebirs7692808
HLIrs7692808
Exacrs7692808
Gnomadrs7692808
Varsomers7692808
LitVarrs7692808
Maprs7692808
PheGenIrs7692808
Biobankrs7692808
1000 genomesrs7692808
hgdprs7692808
ensemblrs7692808
geneviewrs7692808
scholarrs7692808
googlers7692808
pharmgkbrs7692808
gwascentralrs7692808
openSNPrs7692808
23andMers7692808
SNPshotrs7692808
SNPdbers7692808
MSV3drs7692808
GWAS Ctlgrs7692808
GMAF0.3691
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval
Risk Allele A
P-val 6E-20
Odds Ratio 2.01 [1.58-2.44] ms decrease

[PMID 21347284OA-icon.png] Genome-wide association studies of the PR interval in African Americans.