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rs397517497

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517497(A;A)
Make rs397517497(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178790707
GeneTTN
is asnp
is mentioned by
dbSNPrs397517497
ebirs397517497
HLIrs397517497
Exacrs397517497
Varsomers397517497
Maprs397517497
PheGenIrs397517497
hapmaprs397517497
1000 genomesrs397517497
hgdprs397517497
ensemblrs397517497
gopubmedrs397517497
geneviewrs397517497
scholarrs397517497
googlers397517497
pharmgkbrs397517497
gwascentralrs397517497
openSNPrs397517497
23andMers397517497
23andMe allrs397517497
SNP Nexus

SNPshotrs397517497
SNPdbers397517497
MSV3drs397517497
GWAS Ctlgrs397517497
Max Magnitude0
ClinVar
Risk rs397517497(A;A)
Alt rs397517497(A;A)
Reference rs397517497(G;G)
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.179655434C>T
CLNSRC ClinVar
CLNACC RCV000039959.2, RCV000184208.1,