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rs121434298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434298(A;A)
Make rs121434298(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position39665865
GeneTCAP
is asnp
is mentioned by
dbSNPrs121434298
ebirs121434298
HLIrs121434298
Exacrs121434298
Varsomers121434298
Maprs121434298
PheGenIrs121434298
hapmaprs121434298
1000 genomesrs121434298
hgdprs121434298
ensemblrs121434298
gopubmedrs121434298
geneviewrs121434298
scholarrs121434298
googlers121434298
pharmgkbrs121434298
gwascentralrs121434298
openSNPrs121434298
23andMers121434298
23andMe allrs121434298
SNP Nexus

SNPshotrs121434298
SNPdbers121434298
MSV3drs121434298
GWAS Ctlgrs121434298
Max Magnitude0
OMIM604488
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434298(A;A)
Alt rs121434298(A;A)
Reference rs121434298(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1N
Variation info
Gene TCAP
CLNDBN Dilated cardiomyopathy 1N
Reversed 0
HGVS NC_000017.10:g.37822118G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005863.5,