rs6439167
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6439167(C;C) |
Make rs6439167(C;T) |
Make rs6439167(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 129331913 |
is a | snp |
is | mentioned by |
dbSNP | rs6439167 |
dbSNP (classic) | rs6439167 |
ClinGen | rs6439167 |
ebi | rs6439167 |
HLI | rs6439167 |
Exac | rs6439167 |
Gnomad | rs6439167 |
Varsome | rs6439167 |
LitVar | rs6439167 |
Map | rs6439167 |
PheGenI | rs6439167 |
Biobank | rs6439167 |
1000 genomes | rs6439167 |
hgdp | rs6439167 |
ensembl | rs6439167 |
geneview | rs6439167 |
scholar | rs6439167 |
rs6439167 | |
pharmgkb | rs6439167 |
gwascentral | rs6439167 |
openSNP | rs6439167 |
23andMe | rs6439167 |
SNPshot | rs6439167 |
SNPdbe | rs6439167 |
MSV3d | rs6439167 |
GWAS Ctlg | rs6439167 |
GMAF | 0.1515 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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-15 |
Odds Ratio | 0.03 [NR] unit decrease |