rs2287218
From SNPedia
Orientation | minus |
Stabilized | minus |
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 |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 109581533 |
Gene | MVK |
is a | snp |
is | mentioned by |
dbSNP | rs2287218 |
dbSNP (classic) | rs2287218 |
ClinGen | rs2287218 |
ebi | rs2287218 |
HLI | rs2287218 |
Exac | rs2287218 |
Gnomad | rs2287218 |
Varsome | rs2287218 |
LitVar | rs2287218 |
Map | rs2287218 |
PheGenI | rs2287218 |
Biobank | rs2287218 |
1000 genomes | rs2287218 |
hgdp | rs2287218 |
ensembl | rs2287218 |
geneview | rs2287218 |
scholar | rs2287218 |
rs2287218 | |
pharmgkb | rs2287218 |
gwascentral | rs2287218 |
openSNP | rs2287218 |
23andMe | rs2287218 |
SNPshot | rs2287218 |
SNPdbe | rs2287218 |
MSV3d | rs2287218 |
GWAS Ctlg | rs2287218 |
Max Magnitude | 2.6 |
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 |
---|---|---|
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