rs798489
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs798489(A;A) |
Make rs798489(A;G) |
Make rs798489(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 2762169 |
Gene | AMZ1, GNA12 |
is a | snp |
is | mentioned by |
dbSNP | rs798489 |
dbSNP (classic) | rs798489 |
ClinGen | rs798489 |
ebi | rs798489 |
HLI | rs798489 |
Exac | rs798489 |
Gnomad | rs798489 |
Varsome | rs798489 |
LitVar | rs798489 |
Map | rs798489 |
PheGenI | rs798489 |
Biobank | rs798489 |
1000 genomes | rs798489 |
hgdp | rs798489 |
ensembl | rs798489 |
geneview | rs798489 |
scholar | rs798489 |
rs798489 | |
pharmgkb | rs798489 |
gwascentral | rs798489 |
openSNP | rs798489 |
23andMe | rs798489 |
SNPshot | rs798489 |
SNPdbe | rs798489 |
MSV3d | rs798489 |
GWAS Ctlg | rs798489 |
GMAF | 0.1662 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 2E-33 |
Odds Ratio | .05 [NR] unit decrease |