rs961764
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs961764(C;C) |
Make rs961764(C;G) |
Make rs961764(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 117200993 |
is a | snp |
is | mentioned by |
dbSNP | rs961764 |
dbSNP (classic) | rs961764 |
ClinGen | rs961764 |
ebi | rs961764 |
HLI | rs961764 |
Exac | rs961764 |
Gnomad | rs961764 |
Varsome | rs961764 |
LitVar | rs961764 |
Map | rs961764 |
PheGenI | rs961764 |
Biobank | rs961764 |
1000 genomes | rs961764 |
hgdp | rs961764 |
ensembl | rs961764 |
geneview | rs961764 |
scholar | rs961764 |
rs961764 | |
pharmgkb | rs961764 |
gwascentral | rs961764 |
openSNP | rs961764 |
23andMe | rs961764 |
SNPshot | rs961764 |
SNPdbe | rs961764 |
MSV3d | rs961764 |
GWAS Ctlg | rs961764 |
GMAF | 0.3792 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 1E-11 |
Odds Ratio | .02 [NR] unit decrease |