rs13290979
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13290979(A;A) |
Make rs13290979(A;G) |
Make rs13290979(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 136531182 |
Gene | NOTCH1 |
is a | snp |
is | mentioned by |
dbSNP | rs13290979 |
dbSNP (classic) | rs13290979 |
ClinGen | rs13290979 |
ebi | rs13290979 |
HLI | rs13290979 |
Exac | rs13290979 |
Gnomad | rs13290979 |
Varsome | rs13290979 |
LitVar | rs13290979 |
Map | rs13290979 |
PheGenI | rs13290979 |
Biobank | rs13290979 |
1000 genomes | rs13290979 |
hgdp | rs13290979 |
ensembl | rs13290979 |
geneview | rs13290979 |
scholar | rs13290979 |
rs13290979 | |
pharmgkb | rs13290979 |
gwascentral | rs13290979 |
openSNP | rs13290979 |
23andMe | rs13290979 |
SNPshot | rs13290979 |
SNPdbe | rs13290979 |
MSV3d | rs13290979 |
GWAS Ctlg | rs13290979 |
GMAF | 0.4178 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23798201] NOTCH1 genetic variants in patients with tricuspid calcific aortic valve stenosis