rs115015150
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs115015150(C;C) |
Make rs115015150(C;T) |
Make rs115015150(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 150469570 |
Gene | RND3 |
is a | snp |
is | mentioned by |
dbSNP | rs115015150 |
dbSNP (classic) | rs115015150 |
ClinGen | rs115015150 |
ebi | rs115015150 |
HLI | rs115015150 |
Exac | rs115015150 |
Gnomad | rs115015150 |
Varsome | rs115015150 |
LitVar | rs115015150 |
Map | rs115015150 |
PheGenI | rs115015150 |
Biobank | rs115015150 |
1000 genomes | rs115015150 |
hgdp | rs115015150 |
ensembl | rs115015150 |
geneview | rs115015150 |
scholar | rs115015150 |
rs115015150 | |
pharmgkb | rs115015150 |
gwascentral | rs115015150 |
openSNP | rs115015150 |
23andMe | rs115015150 |
SNPshot | rs115015150 |
SNPdbe | rs115015150 |
MSV3d | rs115015150 |
GWAS Ctlg | rs115015150 |
GMAF | 0.008724 |
Max Magnitude | 0 |
[PMID 23420841] Genetic dissection of the preeclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease