rs6473015
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6473015(A;A) |
Make rs6473015(A;C) |
Make rs6473015(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 77266249 |
is a | snp |
is | mentioned by |
dbSNP | rs6473015 |
dbSNP (classic) | rs6473015 |
ClinGen | rs6473015 |
ebi | rs6473015 |
HLI | rs6473015 |
Exac | rs6473015 |
Gnomad | rs6473015 |
Varsome | rs6473015 |
LitVar | rs6473015 |
Map | rs6473015 |
PheGenI | rs6473015 |
Biobank | rs6473015 |
1000 genomes | rs6473015 |
hgdp | rs6473015 |
ensembl | rs6473015 |
geneview | rs6473015 |
scholar | rs6473015 |
rs6473015 | |
pharmgkb | rs6473015 |
gwascentral | rs6473015 |
openSNP | rs6473015 |
23andMe | rs6473015 |
SNPshot | rs6473015 |
SNPdbe | rs6473015 |
MSV3d | rs6473015 |
GWAS Ctlg | rs6473015 |
GMAF | 0.2204 |
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 | A |
P-val | 7E-13 |
Odds Ratio | .03 [NR] unit decrease |