rs7567288
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7567288(C;C) |
Make rs7567288(C;T) |
Make rs7567288(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 133677253 |
is a | snp |
is | mentioned by |
dbSNP | rs7567288 |
dbSNP (classic) | rs7567288 |
ClinGen | rs7567288 |
ebi | rs7567288 |
HLI | rs7567288 |
Exac | rs7567288 |
Gnomad | rs7567288 |
Varsome | rs7567288 |
LitVar | rs7567288 |
Map | rs7567288 |
PheGenI | rs7567288 |
Biobank | rs7567288 |
1000 genomes | rs7567288 |
hgdp | rs7567288 |
ensembl | rs7567288 |
geneview | rs7567288 |
scholar | rs7567288 |
rs7567288 | |
pharmgkb | rs7567288 |
gwascentral | rs7567288 |
openSNP | rs7567288 |
23andMe | rs7567288 |
SNPshot | rs7567288 |
SNPdbe | rs7567288 |
MSV3d | rs7567288 |
GWAS Ctlg | rs7567288 |
GMAF | 0.202 |
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 | 2E-12 |
Odds Ratio | .03 [NR] unit decrease |