rs2780226
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2780226(A;A) |
Make rs2780226(A;G) |
Make rs2780226(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 34231315 |
is a | snp |
is | mentioned by |
dbSNP | rs2780226 |
dbSNP (classic) | rs2780226 |
ClinGen | rs2780226 |
ebi | rs2780226 |
HLI | rs2780226 |
Exac | rs2780226 |
Gnomad | rs2780226 |
Varsome | rs2780226 |
LitVar | rs2780226 |
Map | rs2780226 |
PheGenI | rs2780226 |
Biobank | rs2780226 |
1000 genomes | rs2780226 |
hgdp | rs2780226 |
ensembl | rs2780226 |
geneview | rs2780226 |
scholar | rs2780226 |
rs2780226 | |
pharmgkb | rs2780226 |
gwascentral | rs2780226 |
openSNP | rs2780226 |
23andMe | rs2780226 |
SNPshot | rs2780226 |
SNPdbe | rs2780226 |
MSV3d | rs2780226 |
GWAS Ctlg | rs2780226 |
GMAF | 0.2126 |
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 | 8E-28 |
Odds Ratio | .08 [NR] unit decrease |