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rs397517576

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517576(-;-)
Make rs397517576(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position178629361
GeneTTN
is asnp
is mentioned by
dbSNPrs397517576
ebirs397517576
HLIrs397517576
Exacrs397517576
Varsomers397517576
Maprs397517576
PheGenIrs397517576
hapmaprs397517576
1000 genomesrs397517576
hgdprs397517576
ensemblrs397517576
gopubmedrs397517576
geneviewrs397517576
scholarrs397517576
googlers397517576
pharmgkbrs397517576
gwascentralrs397517576
openSNPrs397517576
23andMers397517576
23andMe allrs397517576
SNP Nexus

SNPshotrs397517576
SNPdbers397517576
MSV3drs397517576
GWAS Ctlgrs397517576
Max Magnitude0
ClinVar
Risk rs397517576(;)
Alt rs397517576(;)
Reference rs397517576(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179494088delG
CLNSRC ClinVar
CLNACC RCV000040246.2,