rs1238566
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1238566(A;A) |
Make rs1238566(A;G) |
Make rs1238566(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 128745591 |
Gene | FLI1 |
is a | snp |
is | mentioned by |
dbSNP | rs1238566 |
dbSNP (classic) | rs1238566 |
ClinGen | rs1238566 |
ebi | rs1238566 |
HLI | rs1238566 |
Exac | rs1238566 |
Gnomad | rs1238566 |
Varsome | rs1238566 |
LitVar | rs1238566 |
Map | rs1238566 |
PheGenI | rs1238566 |
Biobank | rs1238566 |
1000 genomes | rs1238566 |
hgdp | rs1238566 |
ensembl | rs1238566 |
geneview | rs1238566 |
scholar | rs1238566 |
rs1238566 | |
pharmgkb | rs1238566 |
gwascentral | rs1238566 |
openSNP | rs1238566 |
23andMe | rs1238566 |
SNPshot | rs1238566 |
SNPdbe | rs1238566 |
MSV3d | rs1238566 |
GWAS Ctlg | rs1238566 |
GMAF | 0.3912 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24046805] Genome-wide and candidate gene association studies of placental abruption