rs1738475
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1738475(C;C) |
Make rs1738475(C;G) |
Make rs1738475(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 23210398 |
is a | snp |
is | mentioned by |
dbSNP | rs1738475 |
dbSNP (classic) | rs1738475 |
ClinGen | rs1738475 |
ebi | rs1738475 |
HLI | rs1738475 |
Exac | rs1738475 |
Gnomad | rs1738475 |
Varsome | rs1738475 |
LitVar | rs1738475 |
Map | rs1738475 |
PheGenI | rs1738475 |
Biobank | rs1738475 |
1000 genomes | rs1738475 |
hgdp | rs1738475 |
ensembl | rs1738475 |
geneview | rs1738475 |
scholar | rs1738475 |
rs1738475 | |
pharmgkb | rs1738475 |
gwascentral | rs1738475 |
openSNP | rs1738475 |
23andMe | rs1738475 |
SNPshot | rs1738475 |
SNPdbe | rs1738475 |
MSV3d | rs1738475 |
GWAS Ctlg | rs1738475 |
GMAF | 0.4972 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | C |
P-val | 3E-12 |
Odds Ratio | 0.0300 [NR] meters increase |