rs3759387
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3759387(A;A) |
Make rs3759387(A;C) |
Make rs3759387(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 109574662 |
Gene | MMAB, MVK |
is a | snp |
is | mentioned by |
dbSNP | rs3759387 |
dbSNP (classic) | rs3759387 |
ClinGen | rs3759387 |
ebi | rs3759387 |
HLI | rs3759387 |
Exac | rs3759387 |
Gnomad | rs3759387 |
Varsome | rs3759387 |
LitVar | rs3759387 |
Map | rs3759387 |
PheGenI | rs3759387 |
Biobank | rs3759387 |
1000 genomes | rs3759387 |
hgdp | rs3759387 |
ensembl | rs3759387 |
geneview | rs3759387 |
scholar | rs3759387 |
rs3759387 | |
pharmgkb | rs3759387 |
gwascentral | rs3759387 |
openSNP | rs3759387 |
23andMe | rs3759387 |
SNPshot | rs3759387 |
SNPdbe | rs3759387 |
MSV3d | rs3759387 |
GWAS Ctlg | rs3759387 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 29069827] 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.