rs2665838
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2665838(C;C) |
Make rs2665838(C;G) |
Make rs2665838(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 63889105 |
is a | snp |
is | mentioned by |
dbSNP | rs2665838 |
dbSNP (classic) | rs2665838 |
ClinGen | rs2665838 |
ebi | rs2665838 |
HLI | rs2665838 |
Exac | rs2665838 |
Gnomad | rs2665838 |
Varsome | rs2665838 |
LitVar | rs2665838 |
Map | rs2665838 |
PheGenI | rs2665838 |
Biobank | rs2665838 |
1000 genomes | rs2665838 |
hgdp | rs2665838 |
ensembl | rs2665838 |
geneview | rs2665838 |
scholar | rs2665838 |
rs2665838 | |
pharmgkb | rs2665838 |
gwascentral | rs2665838 |
openSNP | rs2665838 |
23andMe | rs2665838 |
SNPshot | rs2665838 |
SNPdbe | rs2665838 |
MSV3d | rs2665838 |
GWAS Ctlg | rs2665838 |
GMAF | 0.1901 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 5E-25 |
Odds Ratio | 0.04 [NR] unit decrease |