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rs3869109

From SNPedia

Orientationminus
Stabilizedminus
Make rs3869109(C;C)
Make rs3869109(C;T)
Make rs3869109(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31216419
is asnp
is mentioned by
dbSNPrs3869109
ebirs3869109
HLIrs3869109
Exacrs3869109
Varsomers3869109
Maprs3869109
PheGenIrs3869109
hapmaprs3869109
1000 genomesrs3869109
hgdprs3869109
ensemblrs3869109
gopubmedrs3869109
geneviewrs3869109
scholarrs3869109
googlers3869109
pharmgkbrs3869109
gwascentralrs3869109
openSNPrs3869109
23andMers3869109
23andMe allrs3869109
SNP Nexus

SNPshotrs3869109
SNPdbers3869109
MSV3drs3869109
GWAS Ctlgrs3869109
GMAF0.4403
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22319020OA-icon.png]
Trait
Title A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
Risk Allele G
P-val 1E-9
Odds Ratio 1.1400 None


[PMID 19107206OA-icon.png] Distinct genetic loci control plasma HIV-RNA and cellular HIV-DNA levels in HIV-1 infection: the ANRS Genome Wide Association 01 study.


[PMID 23266671] A novel major histocompatibility complex locus confers the risk of premature coronary artery disease in a Chinese Han population.