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rs397517689

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517689(C;T)
Make rs397517689(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178574530
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517689
ebirs397517689
HLIrs397517689
Exacrs397517689
Varsomers397517689
Maprs397517689
PheGenIrs397517689
hapmaprs397517689
1000 genomesrs397517689
hgdprs397517689
ensemblrs397517689
gopubmedrs397517689
geneviewrs397517689
scholarrs397517689
googlers397517689
pharmgkbrs397517689
gwascentralrs397517689
openSNPrs397517689
23andMers397517689
23andMe allrs397517689
SNP Nexus

SNPshotrs397517689
SNPdbers397517689
MSV3drs397517689
GWAS Ctlgrs397517689
Max Magnitude0
ClinVar
Risk rs397517689(T;T)
Alt rs397517689(T;T)
Reference rs397517689(C;C)
Significance Other
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179439257G>A
CLNSRC ClinVar
CLNACC RCV000184258.2, RCV000208052.2,