rs13177718
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 |
Make rs13177718(C;T) |
Make rs13177718(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 108777643 |
Gene | FER |
is a | snp |
is | mentioned by |
dbSNP | rs13177718 |
dbSNP (classic) | rs13177718 |
ClinGen | rs13177718 |
ebi | rs13177718 |
HLI | rs13177718 |
Exac | rs13177718 |
Gnomad | rs13177718 |
Varsome | rs13177718 |
LitVar | rs13177718 |
Map | rs13177718 |
PheGenI | rs13177718 |
Biobank | rs13177718 |
1000 genomes | rs13177718 |
hgdp | rs13177718 |
ensembl | rs13177718 |
geneview | rs13177718 |
scholar | rs13177718 |
rs13177718 | |
pharmgkb | rs13177718 |
gwascentral | rs13177718 |
openSNP | rs13177718 |
23andMe | rs13177718 |
SNPshot | rs13177718 |
SNPdbe | rs13177718 |
MSV3d | rs13177718 |
GWAS Ctlg | rs13177718 |
GMAF | 0.03306 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20881960] |
Trait | Height |
Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Risk Allele | T |
P-val | 3E-8 |
Odds Ratio | .04 [NR] unit decrease |