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rs397517589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517589(C;T)
Make rs397517589(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178617845
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517589
ebirs397517589
HLIrs397517589
Exacrs397517589
Varsomers397517589
Maprs397517589
PheGenIrs397517589
hapmaprs397517589
1000 genomesrs397517589
hgdprs397517589
ensemblrs397517589
gopubmedrs397517589
geneviewrs397517589
scholarrs397517589
googlers397517589
pharmgkbrs397517589
gwascentralrs397517589
openSNPrs397517589
23andMers397517589
23andMe allrs397517589
SNP Nexus

SNPshotrs397517589
SNPdbers397517589
MSV3drs397517589
GWAS Ctlgrs397517589
Max Magnitude0
ClinVar
Risk rs397517589(T;T)
Alt rs397517589(T;T)
Reference Rs397517589(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179482572G>A
CLNSRC ClinVar
CLNACC RCV000040282.2,