rs13170645
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13170645(A;A) |
Make rs13170645(A;G) |
Make rs13170645(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 44329101 |
Gene | FGF10 |
is a | snp |
is | mentioned by |
dbSNP | rs13170645 |
dbSNP (classic) | rs13170645 |
ClinGen | rs13170645 |
ebi | rs13170645 |
HLI | rs13170645 |
Exac | rs13170645 |
Gnomad | rs13170645 |
Varsome | rs13170645 |
LitVar | rs13170645 |
Map | rs13170645 |
PheGenI | rs13170645 |
Biobank | rs13170645 |
1000 genomes | rs13170645 |
hgdp | rs13170645 |
ensembl | rs13170645 |
geneview | rs13170645 |
scholar | rs13170645 |
rs13170645 | |
pharmgkb | rs13170645 |
gwascentral | rs13170645 |
openSNP | rs13170645 |
23andMe | rs13170645 |
SNPshot | rs13170645 |
SNPdbe | rs13170645 |
MSV3d | rs13170645 |
GWAS Ctlg | rs13170645 |
GMAF | 0.4844 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22965740] Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies