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rs397517787

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517787(C;T)
Make rs397517787(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178533666
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517787
ebirs397517787
HLIrs397517787
Exacrs397517787
Varsomers397517787
Maprs397517787
PheGenIrs397517787
hapmaprs397517787
1000 genomesrs397517787
hgdprs397517787
ensemblrs397517787
gopubmedrs397517787
geneviewrs397517787
scholarrs397517787
googlers397517787
pharmgkbrs397517787
gwascentralrs397517787
openSNPrs397517787
23andMers397517787
23andMe allrs397517787
SNP Nexus

SNPshotrs397517787
SNPdbers397517787
MSV3drs397517787
GWAS Ctlgrs397517787
Max Magnitude0
ClinVar
Risk rs397517787(T;T)
Alt rs397517787(T;T)
Reference rs397517787(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.179398393G>A
CLNSRC ClinVar
CLNACC RCV000040926.2,