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rs794729285

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729285(C;T)
Make rs794729285(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178571794
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729285
ebirs794729285
HLIrs794729285
Exacrs794729285
Varsomers794729285
Maprs794729285
PheGenIrs794729285
hapmaprs794729285
1000 genomesrs794729285
hgdprs794729285
ensemblrs794729285
gopubmedrs794729285
geneviewrs794729285
scholarrs794729285
googlers794729285
pharmgkbrs794729285
gwascentralrs794729285
openSNPrs794729285
23andMers794729285
23andMe allrs794729285
SNP Nexus

SNPshotrs794729285
SNPdbers794729285
MSV3drs794729285
GWAS Ctlgrs794729285
Max Magnitude0
ClinVar
Risk rs794729285(T;T)
Alt rs794729285(T;T)
Reference rs794729285(C;C)
Significance Probable-Pathogenic
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.179436521G>A
CLNSRC
CLNACC RCV000184261.2, RCV000208904.1,