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rs1445021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in complete genomics
Make rs1445021(C;C)
Make rs1445021(C;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position68443247
is asnp
is mentioned by
dbSNPrs1445021
ebirs1445021
HLIrs1445021
Exacrs1445021
Varsomers1445021
Maprs1445021
PheGenIrs1445021
hapmaprs1445021
1000 genomesrs1445021
hgdprs1445021
ensemblrs1445021
gopubmedrs1445021
geneviewrs1445021
scholarrs1445021
googlers1445021
pharmgkbrs1445021
gwascentralrs1445021
openSNPrs1445021
23andMers1445021
23andMe allrs1445021
SNP Nexus

SNPshotrs1445021
SNPdbers1445021
MSV3drs1445021
GWAS Ctlgrs1445021
GMAF0.01699
Max Magnitude0
? (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 A
P-val 0.000009
Odds Ratio 0.1365 [0.08-0.20] SD increase