rs1013209
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1013209(C;C) |
Make rs1013209(C;T) |
Make rs1013209(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 24258791 |
is a | snp |
is | mentioned by |
dbSNP | rs1013209 |
dbSNP (classic) | rs1013209 |
ClinGen | rs1013209 |
ebi | rs1013209 |
HLI | rs1013209 |
Exac | rs1013209 |
Gnomad | rs1013209 |
Varsome | rs1013209 |
LitVar | rs1013209 |
Map | rs1013209 |
PheGenI | rs1013209 |
Biobank | rs1013209 |
1000 genomes | rs1013209 |
hgdp | rs1013209 |
ensembl | rs1013209 |
geneview | rs1013209 |
scholar | rs1013209 |
rs1013209 | |
pharmgkb | rs1013209 |
gwascentral | rs1013209 |
openSNP | rs1013209 |
23andMe | rs1013209 |
SNPshot | rs1013209 |
SNPdbe | rs1013209 |
MSV3d | rs1013209 |
GWAS Ctlg | rs1013209 |
GMAF | 0.3049 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 2E-9 |
Odds Ratio | 0.0300 [NR] meters decrease |