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rs1899430

From SNPedia

Orientationplus
Stabilizedplus
Make rs1899430(C;C)
Make rs1899430(C;T)
Make rs1899430(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position57915616
is asnp
is mentioned by
dbSNPrs1899430
ebirs1899430
HLIrs1899430
Exacrs1899430
Varsomers1899430
Maprs1899430
PheGenIrs1899430
hapmaprs1899430
1000 genomesrs1899430
hgdprs1899430
ensemblrs1899430
gopubmedrs1899430
geneviewrs1899430
scholarrs1899430
googlers1899430
pharmgkbrs1899430
gwascentralrs1899430
openSNPrs1899430
23andMers1899430
23andMe allrs1899430
SNP Nexus

SNPshotrs1899430
SNPdbers1899430
MSV3drs1899430
GWAS Ctlgrs1899430
GMAF0.1961
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19886994OA-icon.png] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease