rs1960669
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1960669(G;G) |
Make rs1960669(G;T) |
Make rs1960669(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 122861413 |
Gene | FGF2 |
is a | snp |
is | mentioned by |
dbSNP | rs1960669 |
dbSNP (classic) | rs1960669 |
ClinGen | rs1960669 |
ebi | rs1960669 |
HLI | rs1960669 |
Exac | rs1960669 |
Gnomad | rs1960669 |
Varsome | rs1960669 |
LitVar | rs1960669 |
Map | rs1960669 |
PheGenI | rs1960669 |
Biobank | rs1960669 |
1000 genomes | rs1960669 |
hgdp | rs1960669 |
ensembl | rs1960669 |
geneview | rs1960669 |
scholar | rs1960669 |
rs1960669 | |
pharmgkb | rs1960669 |
gwascentral | rs1960669 |
openSNP | rs1960669 |
23andMe | rs1960669 |
SNPshot | rs1960669 |
SNPdbe | rs1960669 |
MSV3d | rs1960669 |
GWAS Ctlg | rs1960669 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 27237708] Variants in genes belonging to the Fibroblast Growth Factor family are associated with lower extremity amputation in non-Hispanic whites: Findings from the Chronic Renal Insufficiency Cohort study.