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rs397517565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517565(-;-)
Make rs397517565(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178635714
GeneTTN
is asnp
is mentioned by
dbSNPrs397517565
ebirs397517565
HLIrs397517565
Exacrs397517565
Varsomers397517565
Maprs397517565
PheGenIrs397517565
hapmaprs397517565
1000 genomesrs397517565
hgdprs397517565
ensemblrs397517565
gopubmedrs397517565
geneviewrs397517565
scholarrs397517565
googlers397517565
pharmgkbrs397517565
gwascentralrs397517565
openSNPrs397517565
23andMers397517565
23andMe allrs397517565
SNP Nexus

SNPshotrs397517565
SNPdbers397517565
MSV3drs397517565
GWAS Ctlgrs397517565
Max Magnitude0
ClinVar
Risk rs397517565(;)
Alt rs397517565(;)
Reference rs397517565(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000002.11:g.179500441delT
CLNSRC ClinVar
CLNACC RCV000040217.2, RCV000184297.1,