Have questions? Visit https://www.reddit.com/r/SNPedia

rs7660702

From SNPedia

Orientationplus
Stabilizedplus
Make rs7660702(C;C)
Make rs7660702(C;T)
Make rs7660702(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position85730311
GeneARHGAP24
is asnp
is mentioned by
dbSNPrs7660702
ebirs7660702
HLIrs7660702
Exacrs7660702
Varsomers7660702
Maprs7660702
PheGenIrs7660702
hapmaprs7660702
1000 genomesrs7660702
hgdprs7660702
ensemblrs7660702
gopubmedrs7660702
geneviewrs7660702
scholarrs7660702
googlers7660702
pharmgkbrs7660702
gwascentralrs7660702
openSNPrs7660702
23andMers7660702
23andMe allrs7660702
SNP Nexus

SNPshotrs7660702
SNPdbers7660702
MSV3drs7660702
GWAS Ctlgrs7660702
GMAF0.4284
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20062063]
Trait Electrocardiographic traits
Title Several common variants modulate heart rate, PR interval and QRS duration
Risk Allele T
P-val 3E-17
Odds Ratio 8.46 [6.50-10.42] % SD increase

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