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rs2287218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 2.6 Slightly higher risk for CHD and IS
(A;G) 1.6 Slightly higher risk for CHD and IS
(G;G) 0 common/normal
ReferenceGRCh38.p7 38.3/151
Chromosome12
Position109581533
GeneMVK
is asnp
is mentioned by
dbSNPrs2287218
dbSNP (classic)rs2287218
ClinGenrs2287218
ebirs2287218
HLIrs2287218
Exacrs2287218
Gnomadrs2287218
Varsomers2287218
LitVarrs2287218
Maprs2287218
PheGenIrs2287218
Biobankrs2287218
1000 genomesrs2287218
hgdprs2287218
ensemblrs2287218
geneviewrs2287218
scholarrs2287218
googlers2287218
pharmgkbrs2287218
gwascentralrs2287218
openSNPrs2287218
23andMers2287218
SNPshotrs2287218
SNPdbers2287218
MSV3drs2287218
GWAS Ctlgrs2287218
Max Magnitude2.6

Based on a study of 1764 unrelated Southern Han Chinese subjects (CHD, 583; IS, 555; and healthy controls, 626), rs2287218(A) allele carriers had an increased risk of coronary heart disease and ischemic stroke (CHD: OR = 1.674, CI: 1.25-2.25, p = 0.001 for AG/AA vs. GG genotypes; IS: OR = 1.890, CI: 1.36-2.47, p = 0.001 for AG/AA vs. GG genotypes). The authors hypothesize that rs2287218 is likely to increase the risk of CHD and IS by decreasing serum HDL-C levels.[PMID 30101835]

? (A;A) (A;G) (G;G) 28