rs3110496
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3110496(A;A) |
Make rs3110496(A;G) |
Make rs3110496(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 29590753 |
Gene | ANKRD13B, GIT1 |
is a | snp |
is | mentioned by |
dbSNP | rs3110496 |
dbSNP (classic) | rs3110496 |
ClinGen | rs3110496 |
ebi | rs3110496 |
HLI | rs3110496 |
Exac | rs3110496 |
Gnomad | rs3110496 |
Varsome | rs3110496 |
LitVar | rs3110496 |
Map | rs3110496 |
PheGenI | rs3110496 |
Biobank | rs3110496 |
1000 genomes | rs3110496 |
hgdp | rs3110496 |
ensembl | rs3110496 |
geneview | rs3110496 |
scholar | rs3110496 |
rs3110496 | |
pharmgkb | rs3110496 |
gwascentral | rs3110496 |
openSNP | rs3110496 |
23andMe | rs3110496 |
SNPshot | rs3110496 |
SNPdbe | rs3110496 |
MSV3d | rs3110496 |
GWAS Ctlg | rs3110496 |
GMAF | 0.3118 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | A |
P-val | 7E-9 |
Odds Ratio | 0.0200 [NR] meters decrease |