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rs397517547

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517547(C;T)
Make rs397517547(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178782872
GeneTTN
is asnp
is mentioned by
dbSNPrs397517547
ebirs397517547
HLIrs397517547
Exacrs397517547
Varsomers397517547
Maprs397517547
PheGenIrs397517547
hapmaprs397517547
1000 genomesrs397517547
hgdprs397517547
ensemblrs397517547
gopubmedrs397517547
geneviewrs397517547
scholarrs397517547
googlers397517547
pharmgkbrs397517547
gwascentralrs397517547
openSNPrs397517547
23andMers397517547
23andMe allrs397517547
SNP Nexus

SNPshotrs397517547
SNPdbers397517547
MSV3drs397517547
GWAS Ctlgrs397517547
Max Magnitude0
ClinVar
Risk rs397517547(T;T)
Alt rs397517547(T;T)
Reference rs397517547(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179647599G>A
CLNSRC ClinVar
CLNACC RCV000040169.3,