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rs1028771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1028771(A;C)
Make rs1028771(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position183201813
GeneLAMC2
is asnp
is mentioned by
dbSNPrs1028771
ebirs1028771
HLIrs1028771
Exacrs1028771
Varsomers1028771
Maprs1028771
PheGenIrs1028771
hapmaprs1028771
1000 genomesrs1028771
hgdprs1028771
ensemblrs1028771
gopubmedrs1028771
geneviewrs1028771
scholarrs1028771
googlers1028771
pharmgkbrs1028771
gwascentralrs1028771
openSNPrs1028771
23andMers1028771
23andMe allrs1028771
SNP Nexus

SNPshotrs1028771
SNPdbers1028771
MSV3drs1028771
GWAS Ctlgrs1028771
GMAF0.009183
Max Magnitude0
? (A;A) (A;C) (C;C) 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 0.000004
Odds Ratio 0.2188 [0.13-0.31] SD decrease