rs2145272
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2145272(A;A) |
Make rs2145272(A;G) |
Make rs2145272(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 6645571 |
is a | snp |
is | mentioned by |
dbSNP | rs2145272 |
dbSNP (classic) | rs2145272 |
ClinGen | rs2145272 |
ebi | rs2145272 |
HLI | rs2145272 |
Exac | rs2145272 |
Gnomad | rs2145272 |
Varsome | rs2145272 |
LitVar | rs2145272 |
Map | rs2145272 |
PheGenI | rs2145272 |
Biobank | rs2145272 |
1000 genomes | rs2145272 |
hgdp | rs2145272 |
ensembl | rs2145272 |
geneview | rs2145272 |
scholar | rs2145272 |
rs2145272 | |
pharmgkb | rs2145272 |
gwascentral | rs2145272 |
openSNP | rs2145272 |
23andMe | rs2145272 |
SNPshot | rs2145272 |
SNPdbe | rs2145272 |
MSV3d | rs2145272 |
GWAS Ctlg | rs2145272 |
GMAF | 0.292 |
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 | A |
P-val | 2E-24 |
Odds Ratio | .04 [NR] unit decrease |