rs487591
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs487591(A;A) |
Make rs487591(A;G) |
Make rs487591(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 225569049 |
Gene | ENAH |
is a | snp |
is | mentioned by |
dbSNP | rs487591 |
dbSNP (classic) | rs487591 |
ClinGen | rs487591 |
ebi | rs487591 |
HLI | rs487591 |
Exac | rs487591 |
Gnomad | rs487591 |
Varsome | rs487591 |
LitVar | rs487591 |
Map | rs487591 |
PheGenI | rs487591 |
Biobank | rs487591 |
1000 genomes | rs487591 |
hgdp | rs487591 |
ensembl | rs487591 |
geneview | rs487591 |
scholar | rs487591 |
rs487591 | |
pharmgkb | rs487591 |
gwascentral | rs487591 |
openSNP | rs487591 |
23andMe | rs487591 |
SNPshot | rs487591 |
SNPdbe | rs487591 |
MSV3d | rs487591 |
GWAS Ctlg | rs487591 |
GMAF | 0.2718 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19641378] The enabled homolog gene polymorphisms are associated with susceptibility and progression of childhood IgA nephropathy