rs288979
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs288979(A;A) |
Make rs288979(A;G) |
Make rs288979(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 21031282 |
Gene | ROCK1 |
is a | snp |
is | mentioned by |
dbSNP | rs288979 |
dbSNP (classic) | rs288979 |
ClinGen | rs288979 |
ebi | rs288979 |
HLI | rs288979 |
Exac | rs288979 |
Gnomad | rs288979 |
Varsome | rs288979 |
LitVar | rs288979 |
Map | rs288979 |
PheGenI | rs288979 |
Biobank | rs288979 |
1000 genomes | rs288979 |
hgdp | rs288979 |
ensembl | rs288979 |
geneview | rs288979 |
scholar | rs288979 |
rs288979 | |
pharmgkb | rs288979 |
gwascentral | rs288979 |
openSNP | rs288979 |
23andMe | rs288979 |
SNPshot | rs288979 |
SNPdbe | rs288979 |
MSV3d | rs288979 |
GWAS Ctlg | rs288979 |
GMAF | 0.2222 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23782575] Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot
[PMID 18205893] Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations.