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rs794729265

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729265(C;T)
Make rs794729265(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178612355
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729265
ebirs794729265
HLIrs794729265
Exacrs794729265
Varsomers794729265
Maprs794729265
PheGenIrs794729265
hapmaprs794729265
1000 genomesrs794729265
hgdprs794729265
ensemblrs794729265
gopubmedrs794729265
geneviewrs794729265
scholarrs794729265
googlers794729265
pharmgkbrs794729265
gwascentralrs794729265
openSNPrs794729265
23andMers794729265
23andMe allrs794729265
SNP Nexus

SNPshotrs794729265
SNPdbers794729265
MSV3drs794729265
GWAS Ctlgrs794729265
Max Magnitude0
ClinVar
Risk rs794729265(T;T)
Alt rs794729265(T;T)
Reference rs794729265(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.179477082G>A
CLNSRC
CLNACC RCV000184225.1, RCV000209230.1,