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rs397517696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517696(-;-)
Make rs397517696(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178572287
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517696
ebirs397517696
HLIrs397517696
Exacrs397517696
Varsomers397517696
Maprs397517696
PheGenIrs397517696
hapmaprs397517696
1000 genomesrs397517696
hgdprs397517696
ensemblrs397517696
gopubmedrs397517696
geneviewrs397517696
scholarrs397517696
googlers397517696
pharmgkbrs397517696
gwascentralrs397517696
openSNPrs397517696
23andMers397517696
23andMe allrs397517696
SNP Nexus

SNPshotrs397517696
SNPdbers397517696
MSV3drs397517696
GWAS Ctlgrs397517696
Max Magnitude0
ClinVar
Risk rs397517696(;)
Alt rs397517696(;)
Reference rs397517696(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179437014delT
CLNSRC ClinVar
CLNACC RCV000040594.2,