rs788867
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs788867(A;A) |
Make rs788867(A;C) |
Make rs788867(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 81228852 |
is a | snp |
is | mentioned by |
dbSNP | rs788867 |
dbSNP (classic) | rs788867 |
ClinGen | rs788867 |
ebi | rs788867 |
HLI | rs788867 |
Exac | rs788867 |
Gnomad | rs788867 |
Varsome | rs788867 |
LitVar | rs788867 |
Map | rs788867 |
PheGenI | rs788867 |
Biobank | rs788867 |
1000 genomes | rs788867 |
hgdp | rs788867 |
ensembl | rs788867 |
geneview | rs788867 |
scholar | rs788867 |
rs788867 | |
pharmgkb | rs788867 |
gwascentral | rs788867 |
openSNP | rs788867 |
23andMe | rs788867 |
SNPshot | rs788867 |
SNPdbe | rs788867 |
MSV3d | rs788867 |
GWAS Ctlg | rs788867 |
GMAF | 0.3623 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 9E-28 |
Odds Ratio | 0.04 [NR] unit decrease |