rs1899430
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1899430(C;C) |
Make rs1899430(C;T) |
Make rs1899430(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 57915616 |
is a | snp |
is | mentioned by |
dbSNP | rs1899430 |
dbSNP (classic) | rs1899430 |
ClinGen | rs1899430 |
ebi | rs1899430 |
HLI | rs1899430 |
Exac | rs1899430 |
Gnomad | rs1899430 |
Varsome | rs1899430 |
LitVar | rs1899430 |
Map | rs1899430 |
PheGenI | rs1899430 |
Biobank | rs1899430 |
1000 genomes | rs1899430 |
hgdp | rs1899430 |
ensembl | rs1899430 |
geneview | rs1899430 |
scholar | rs1899430 |
rs1899430 | |
pharmgkb | rs1899430 |
gwascentral | rs1899430 |
openSNP | rs1899430 |
23andMe | rs1899430 |
SNPshot | rs1899430 |
SNPdbe | rs1899430 |
MSV3d | rs1899430 |
GWAS Ctlg | rs1899430 |
GMAF | 0.1961 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19886994] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease