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rs7134594

From SNPedia

Orientationplus
Stabilizedplus
Make rs7134594(C;C)
Make rs7134594(C;T)
Make rs7134594(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position109562388
GeneMMAB
is asnp
is mentioned by
dbSNPrs7134594
dbSNP (classic)rs7134594
ClinGenrs7134594
ebirs7134594
HLIrs7134594
Exacrs7134594
Gnomadrs7134594
Varsomers7134594
LitVarrs7134594
Maprs7134594
PheGenIrs7134594
Biobankrs7134594
1000 genomesrs7134594
hgdprs7134594
ensemblrs7134594
geneviewrs7134594
scholarrs7134594
googlers7134594
pharmgkbrs7134594
gwascentralrs7134594
openSNPrs7134594
23andMers7134594
SNPshotrs7134594
SNPdbers7134594
MSV3drs7134594
GWAS Ctlgrs7134594
GMAF0.4858
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele C
P-val 7E-15
Odds Ratio 0.4400 None
GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait HDL cholesterol
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele C
P-val 2E-13
Odds Ratio .04 [NR] unit decrease


[PMID 29069827OA-icon.png] The effect of MVK-MMAB variants, their haplotypes and G×E interactions on serum lipid levels and the risk of coronary heart disease and ischemic stroke.