rs8052560
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8052560(A;A) |
Make rs8052560(A;C) |
Make rs8052560(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 88710834 |
Gene | CTU2 |
is a | snp |
is | mentioned by |
dbSNP | rs8052560 |
dbSNP (classic) | rs8052560 |
ClinGen | rs8052560 |
ebi | rs8052560 |
HLI | rs8052560 |
Exac | rs8052560 |
Gnomad | rs8052560 |
Varsome | rs8052560 |
LitVar | rs8052560 |
Map | rs8052560 |
PheGenI | rs8052560 |
Biobank | rs8052560 |
1000 genomes | rs8052560 |
hgdp | rs8052560 |
ensembl | rs8052560 |
geneview | rs8052560 |
scholar | rs8052560 |
rs8052560 | |
pharmgkb | rs8052560 |
gwascentral | rs8052560 |
openSNP | rs8052560 |
23andMe | rs8052560 |
SNPshot | rs8052560 |
SNPdbe | rs8052560 |
MSV3d | rs8052560 |
GWAS Ctlg | rs8052560 |
GMAF | 0.1777 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 3E-8 |
Odds Ratio | .03 [NR] unit increase |