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rs397517601

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517601(A;A)
Make rs397517601(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178611611
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517601
ebirs397517601
HLIrs397517601
Exacrs397517601
Varsomers397517601
Maprs397517601
PheGenIrs397517601
hapmaprs397517601
1000 genomesrs397517601
hgdprs397517601
ensemblrs397517601
gopubmedrs397517601
geneviewrs397517601
scholarrs397517601
googlers397517601
pharmgkbrs397517601
gwascentralrs397517601
openSNPrs397517601
23andMers397517601
23andMe allrs397517601
SNP Nexus

SNPshotrs397517601
SNPdbers397517601
MSV3drs397517601
GWAS Ctlgrs397517601
Max Magnitude0
ClinVar
Risk rs397517601(A;A)
Alt rs397517601(A;A)
Reference rs397517601(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179476338C>T
CLNSRC ClinVar
CLNACC RCV000040317.2,