rs822552
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs822552(C;C) |
Make rs822552(C;G) |
Make rs822552(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 148953542 |
is a | snp |
is | mentioned by |
dbSNP | rs822552 |
dbSNP (classic) | rs822552 |
ClinGen | rs822552 |
ebi | rs822552 |
HLI | rs822552 |
Exac | rs822552 |
Gnomad | rs822552 |
Varsome | rs822552 |
LitVar | rs822552 |
Map | rs822552 |
PheGenI | rs822552 |
Biobank | rs822552 |
1000 genomes | rs822552 |
hgdp | rs822552 |
ensembl | rs822552 |
geneview | rs822552 |
scholar | rs822552 |
rs822552 | |
pharmgkb | rs822552 |
gwascentral | rs822552 |
openSNP | rs822552 |
23andMe | rs822552 |
SNPshot | rs822552 |
SNPdbe | rs822552 |
MSV3d | rs822552 |
GWAS Ctlg | rs822552 |
GMAF | 0.2796 |
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 | 3E-8 |
Odds Ratio | .03 [NR] unit decrease |