rs1530293
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1530293(A;A) |
Make rs1530293(A;G) |
Make rs1530293(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 57918200 |
is a | snp |
is | mentioned by |
dbSNP | rs1530293 |
dbSNP (classic) | rs1530293 |
ClinGen | rs1530293 |
ebi | rs1530293 |
HLI | rs1530293 |
Exac | rs1530293 |
Gnomad | rs1530293 |
Varsome | rs1530293 |
LitVar | rs1530293 |
Map | rs1530293 |
PheGenI | rs1530293 |
Biobank | rs1530293 |
1000 genomes | rs1530293 |
hgdp | rs1530293 |
ensembl | rs1530293 |
geneview | rs1530293 |
scholar | rs1530293 |
rs1530293 | |
pharmgkb | rs1530293 |
gwascentral | rs1530293 |
openSNP | rs1530293 |
23andMe | rs1530293 |
SNPshot | rs1530293 |
SNPdbe | rs1530293 |
MSV3d | rs1530293 |
GWAS Ctlg | rs1530293 |
GMAF | 0.2498 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19886994] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease