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

rs4665630

From SNPedia

Orientationplus
Stabilizedplus
Make rs4665630(C;C)
Make rs4665630(C;T)
Make rs4665630(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position23675447
GeneKLHL29
is asnp
is mentioned by
dbSNPrs4665630
ebirs4665630
HLIrs4665630
Exacrs4665630
Varsomers4665630
Maprs4665630
PheGenIrs4665630
hapmaprs4665630
1000 genomesrs4665630
hgdprs4665630
ensemblrs4665630
gopubmedrs4665630
geneviewrs4665630
scholarrs4665630
googlers4665630
pharmgkbrs4665630
gwascentralrs4665630
openSNPrs4665630
23andMers4665630
23andMe allrs4665630
SNP Nexus

SNPshotrs4665630
SNPdbers4665630
MSV3drs4665630
GWAS Ctlgrs4665630
GMAF0.1846
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele
P-val 1E-7
Odds Ratio 1.2100 [1.13-1.30]