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rs794729278

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729278(C;T)
Make rs794729278(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178590170
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729278
ebirs794729278
HLIrs794729278
Exacrs794729278
Varsomers794729278
Maprs794729278
PheGenIrs794729278
hapmaprs794729278
1000 genomesrs794729278
hgdprs794729278
ensemblrs794729278
gopubmedrs794729278
geneviewrs794729278
scholarrs794729278
googlers794729278
pharmgkbrs794729278
gwascentralrs794729278
openSNPrs794729278
23andMers794729278
23andMe allrs794729278
SNP Nexus

SNPshotrs794729278
SNPdbers794729278
MSV3drs794729278
GWAS Ctlgrs794729278
Max Magnitude0
ClinVar
Risk rs794729278(T;T)
Alt rs794729278(T;T)
Reference rs794729278(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179454897G>A
CLNSRC
CLNACC RCV000184246.1,