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rs2704188

From SNPedia

Orientationminus
Stabilizedminus
Make rs2704188(C;C)
Make rs2704188(C;T)
Make rs2704188(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position58079484
is asnp
is mentioned by
dbSNPrs2704188
dbSNP (old)rs2704188
ClinGenrs2704188
ebirs2704188
HLIrs2704188
Exacrs2704188
Gnomadrs2704188
Varsomers2704188
Maprs2704188
PheGenIrs2704188
Biobankrs2704188
1000 genomesrs2704188
hgdprs2704188
ensemblrs2704188
gopubmedrs2704188
geneviewrs2704188
scholarrs2704188
googlers2704188
pharmgkbrs2704188
gwascentralrs2704188
openSNPrs2704188
23andMers2704188
23andMe allrs2704188
SNP Nexus

SNPshotrs2704188
SNPdbers2704188
MSV3drs2704188
GWAS Ctlgrs2704188
GMAF0.4096
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19886994OA-icon.png] ALDH1A2 (RALDH2) genetic variation in human congenital heart disease