rs2272996
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2272996(C;C) |
Make rs2272996(C;T) |
Make rs2272996(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 132694132 |
Gene | VNN1 |
is a | snp |
is | mentioned by |
dbSNP | rs2272996 |
dbSNP (classic) | rs2272996 |
ClinGen | rs2272996 |
ebi | rs2272996 |
HLI | rs2272996 |
Exac | rs2272996 |
Gnomad | rs2272996 |
Varsome | rs2272996 |
LitVar | rs2272996 |
Map | rs2272996 |
PheGenI | rs2272996 |
Biobank | rs2272996 |
1000 genomes | rs2272996 |
hgdp | rs2272996 |
ensembl | rs2272996 |
geneview | rs2272996 |
scholar | rs2272996 |
rs2272996 | |
pharmgkb | rs2272996 |
gwascentral | rs2272996 |
openSNP | rs2272996 |
23andMe | rs2272996 |
SNPshot | rs2272996 |
SNPdbe | rs2272996 |
MSV3d | rs2272996 |
GWAS Ctlg | rs2272996 |
GMAF | 0.2736 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18043751] Admixture Mapping Provides Evidence of Association of the VNN1 Gene with Hypertension
[PMID 25233454] The Association of the Vanin-1 N131S Variant with Blood Pressure Is Mediated by Endoplasmic Reticulum-Associated Degradation and Loss of Function