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rs397517580

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517580(C;T)
Make rs397517580(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178621517
GeneTTN
is asnp
is mentioned by
dbSNPrs397517580
ebirs397517580
HLIrs397517580
Exacrs397517580
Varsomers397517580
Maprs397517580
PheGenIrs397517580
hapmaprs397517580
1000 genomesrs397517580
hgdprs397517580
ensemblrs397517580
gopubmedrs397517580
geneviewrs397517580
scholarrs397517580
googlers397517580
pharmgkbrs397517580
gwascentralrs397517580
openSNPrs397517580
23andMers397517580
23andMe allrs397517580
SNP Nexus

SNPshotrs397517580
SNPdbers397517580
MSV3drs397517580
GWAS Ctlgrs397517580
Max Magnitude0
ClinVar
Risk rs397517580(T;T)
Alt rs397517580(T;T)
Reference rs397517580(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179486244G>A
CLNSRC ClinVar
CLNACC RCV000040256.2,