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rs794729279

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729279(C;T)
Make rs794729279(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178587684
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729279
ebirs794729279
HLIrs794729279
Exacrs794729279
Varsomers794729279
Maprs794729279
PheGenIrs794729279
hapmaprs794729279
1000 genomesrs794729279
hgdprs794729279
ensemblrs794729279
gopubmedrs794729279
geneviewrs794729279
scholarrs794729279
googlers794729279
pharmgkbrs794729279
gwascentralrs794729279
openSNPrs794729279
23andMers794729279
23andMe allrs794729279
SNP Nexus

SNPshotrs794729279
SNPdbers794729279
MSV3drs794729279
GWAS Ctlgrs794729279
Max Magnitude0
ClinVar
Risk rs794729279(T;T)
Alt rs794729279(T;T)
Reference rs794729279(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179452411G>A
CLNSRC
CLNACC RCV000184249.1,