rs9349655
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9349655(C;C) |
Make rs9349655(C;G) |
Make rs9349655(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 53131910 |
Gene | GCM1 |
is a | snp |
is | mentioned by |
dbSNP | rs9349655 |
dbSNP (classic) | rs9349655 |
ClinGen | rs9349655 |
ebi | rs9349655 |
HLI | rs9349655 |
Exac | rs9349655 |
Gnomad | rs9349655 |
Varsome | rs9349655 |
LitVar | rs9349655 |
Map | rs9349655 |
PheGenI | rs9349655 |
Biobank | rs9349655 |
1000 genomes | rs9349655 |
hgdp | rs9349655 |
ensembl | rs9349655 |
geneview | rs9349655 |
scholar | rs9349655 |
rs9349655 | |
pharmgkb | rs9349655 |
gwascentral | rs9349655 |
openSNP | rs9349655 |
23andMe | rs9349655 |
SNPshot | rs9349655 |
SNPdbe | rs9349655 |
MSV3d | rs9349655 |
GWAS Ctlg | rs9349655 |
GMAF | 0.1148 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 21915358] A fetal variant in the GCM1 gene is associated with pregnancy induced hypertension in a predominantly hispanic population