rs227724
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs227724(A;A) |
Make rs227724(A;T) |
Make rs227724(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 56701456 |
is a | snp |
is | mentioned by |
dbSNP | rs227724 |
dbSNP (classic) | rs227724 |
ClinGen | rs227724 |
ebi | rs227724 |
HLI | rs227724 |
Exac | rs227724 |
Gnomad | rs227724 |
Varsome | rs227724 |
LitVar | rs227724 |
Map | rs227724 |
PheGenI | rs227724 |
Biobank | rs227724 |
1000 genomes | rs227724 |
hgdp | rs227724 |
ensembl | rs227724 |
geneview | rs227724 |
scholar | rs227724 |
rs227724 | |
pharmgkb | rs227724 |
gwascentral | rs227724 |
openSNP | rs227724 |
23andMe | rs227724 |
SNPshot | rs227724 |
SNPdbe | rs227724 |
MSV3d | rs227724 |
GWAS Ctlg | rs227724 |
GMAF | 0.2998 |
Max Magnitude | 0 |
? | (A;A) (A;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 | A |
P-val | 7E-15 |
Odds Ratio | .03 [NR] unit decrease |