rs1173727
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1173727(A;A) |
Make rs1173727(A;G) |
Make rs1173727(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 32830415 |
is a | snp |
is | mentioned by |
dbSNP | rs1173727 |
dbSNP (classic) | rs1173727 |
ClinGen | rs1173727 |
ebi | rs1173727 |
HLI | rs1173727 |
Exac | rs1173727 |
Gnomad | rs1173727 |
Varsome | rs1173727 |
LitVar | rs1173727 |
Map | rs1173727 |
PheGenI | rs1173727 |
Biobank | rs1173727 |
1000 genomes | rs1173727 |
hgdp | rs1173727 |
ensembl | rs1173727 |
geneview | rs1173727 |
scholar | rs1173727 |
rs1173727 | |
pharmgkb | rs1173727 |
gwascentral | rs1173727 |
openSNP | rs1173727 |
23andMe | rs1173727 |
SNPshot | rs1173727 |
SNPdbe | rs1173727 |
MSV3d | rs1173727 |
GWAS Ctlg | rs1173727 |
GMAF | 0.3462 |
Max Magnitude | 0 |
? | (A;A) (A;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 | T |
P-val | 2E-21 |
Odds Ratio | .03 [NR] unit increase |