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rs794729280

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729280(C;T)
Make rs794729280(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178584552
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729280
ebirs794729280
HLIrs794729280
Exacrs794729280
Varsomers794729280
Maprs794729280
PheGenIrs794729280
hapmaprs794729280
1000 genomesrs794729280
hgdprs794729280
ensemblrs794729280
gopubmedrs794729280
geneviewrs794729280
scholarrs794729280
googlers794729280
pharmgkbrs794729280
gwascentralrs794729280
openSNPrs794729280
23andMers794729280
23andMe allrs794729280
SNP Nexus

SNPshotrs794729280
SNPdbers794729280
MSV3drs794729280
GWAS Ctlgrs794729280
Max Magnitude0
ClinVar
Risk rs794729280(T;T)
Alt rs794729280(T;T)
Reference rs794729280(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179449279G>A
CLNSRC
CLNACC RCV000184250.1,