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rs794729381

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729381(G;T)
Make rs794729381(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178574569
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729381
ebirs794729381
HLIrs794729381
Exacrs794729381
Varsomers794729381
Maprs794729381
PheGenIrs794729381
hapmaprs794729381
1000 genomesrs794729381
hgdprs794729381
ensemblrs794729381
gopubmedrs794729381
geneviewrs794729381
scholarrs794729381
googlers794729381
pharmgkbrs794729381
gwascentralrs794729381
openSNPrs794729381
23andMers794729381
23andMe allrs794729381
SNP Nexus

SNPshotrs794729381
SNPdbers794729381
MSV3drs794729381
GWAS Ctlgrs794729381
Max Magnitude0
ClinVar
Risk rs794729381(T;T)
Alt rs794729381(T;T)
Reference rs794729381(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179439296C>A
CLNSRC
CLNACC RCV000184389.1,