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rs1530293

From SNPedia

Orientationplus
Stabilizedplus
Make rs1530293(A;A)
Make rs1530293(A;G)
Make rs1530293(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position57918200
is asnp
is mentioned by
dbSNPrs1530293
dbSNP (classic)rs1530293
ClinGenrs1530293
ebirs1530293
HLIrs1530293
Exacrs1530293
Gnomadrs1530293
Varsomers1530293
LitVarrs1530293
Maprs1530293
PheGenIrs1530293
Biobankrs1530293
1000 genomesrs1530293
hgdprs1530293
ensemblrs1530293
geneviewrs1530293
scholarrs1530293
googlers1530293
pharmgkbrs1530293
gwascentralrs1530293
openSNPrs1530293
23andMers1530293
SNPshotrs1530293
SNPdbers1530293
MSV3drs1530293
GWAS Ctlgrs1530293
GMAF0.2498
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19886994OA-icon.png] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease