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

rs3894944

From SNPedia

Orientationminus
Stabilizedminus
Make rs3894944(C;C)
Make rs3894944(C;T)
Make rs3894944(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position7157975
is asnp
is mentioned by
dbSNPrs3894944
dbSNP (classic)rs3894944
ClinGenrs3894944
ebirs3894944
HLIrs3894944
Exacrs3894944
Gnomadrs3894944
Varsomers3894944
LitVarrs3894944
Maprs3894944
PheGenIrs3894944
Biobankrs3894944
1000 genomesrs3894944
hgdprs3894944
ensemblrs3894944
geneviewrs3894944
scholarrs3894944
googlers3894944
pharmgkbrs3894944
gwascentralrs3894944
openSNPrs3894944
23andMers3894944
SNPshotrs3894944
SNPdbers3894944
MSV3drs3894944
GWAS Ctlgrs3894944
GMAF0.2094
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele A
P-val 3E-6
Odds Ratio .18 [0.1-0.26] unit increase