rs9835332
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9835332(C;C) |
Make rs9835332(C;G) |
Make rs9835332(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 56633654 |
Gene | FAM208A |
is a | snp |
is | mentioned by |
dbSNP | rs9835332 |
dbSNP (classic) | rs9835332 |
ClinGen | rs9835332 |
ebi | rs9835332 |
HLI | rs9835332 |
Exac | rs9835332 |
Gnomad | rs9835332 |
Varsome | rs9835332 |
LitVar | rs9835332 |
Map | rs9835332 |
PheGenI | rs9835332 |
Biobank | rs9835332 |
1000 genomes | rs9835332 |
hgdp | rs9835332 |
ensembl | rs9835332 |
geneview | rs9835332 |
scholar | rs9835332 |
rs9835332 | |
pharmgkb | rs9835332 |
gwascentral | rs9835332 |
openSNP | rs9835332 |
23andMe | rs9835332 |
SNPshot | rs9835332 |
SNPdbe | rs9835332 |
MSV3d | rs9835332 |
GWAS Ctlg | rs9835332 |
GMAF | 0.2833 |
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-13 |
Odds Ratio | 0.03 [NR] unit decrease |
[PMID 31312377] Functional DNA variations associated with Saudi female with low VO2max: a pilot microarray study.