rs2072153
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2072153(C;C) |
Make rs2072153(C;G) |
Make rs2072153(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 49312652 |
Gene | ZNF652 |
is a | snp |
is | mentioned by |
dbSNP | rs2072153 |
dbSNP (classic) | rs2072153 |
ClinGen | rs2072153 |
ebi | rs2072153 |
HLI | rs2072153 |
Exac | rs2072153 |
Gnomad | rs2072153 |
Varsome | rs2072153 |
LitVar | rs2072153 |
Map | rs2072153 |
PheGenI | rs2072153 |
Biobank | rs2072153 |
1000 genomes | rs2072153 |
hgdp | rs2072153 |
ensembl | rs2072153 |
geneview | rs2072153 |
scholar | rs2072153 |
rs2072153 | |
pharmgkb | rs2072153 |
gwascentral | rs2072153 |
openSNP | rs2072153 |
23andMe | rs2072153 |
SNPshot | rs2072153 |
SNPdbe | rs2072153 |
MSV3d | rs2072153 |
GWAS Ctlg | rs2072153 |
GMAF | 0.3209 |
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 | 4E-8 |
Odds Ratio | .02 [NR] unit increase |