rs7652177
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7652177(C;C) |
Make rs7652177(C;G) |
Make rs7652177(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 172251287 |
Gene | FNDC3B |
is a | snp |
is | mentioned by |
dbSNP | rs7652177 |
dbSNP (classic) | rs7652177 |
ClinGen | rs7652177 |
ebi | rs7652177 |
HLI | rs7652177 |
Exac | rs7652177 |
Gnomad | rs7652177 |
Varsome | rs7652177 |
LitVar | rs7652177 |
Map | rs7652177 |
PheGenI | rs7652177 |
Biobank | rs7652177 |
1000 genomes | rs7652177 |
hgdp | rs7652177 |
ensembl | rs7652177 |
geneview | rs7652177 |
scholar | rs7652177 |
rs7652177 | |
pharmgkb | rs7652177 |
gwascentral | rs7652177 |
openSNP | rs7652177 |
23andMe | rs7652177 |
SNPshot | rs7652177 |
SNPdbe | rs7652177 |
MSV3d | rs7652177 |
GWAS Ctlg | rs7652177 |
GMAF | 0.3884 |
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 | |
P-val | 7E-11 |
Odds Ratio | NR NR |