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rs794729366

From SNPedia

Orientationminus
Geno Mag Summary
(TTT;TTT) 0 common in clinvar
Make rs794729366(A;A)
Make rs794729366(A;TTT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178541543
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729366
ebirs794729366
HLIrs794729366
Exacrs794729366
Varsomers794729366
Maprs794729366
PheGenIrs794729366
hapmaprs794729366
1000 genomesrs794729366
hgdprs794729366
ensemblrs794729366
gopubmedrs794729366
geneviewrs794729366
scholarrs794729366
googlers794729366
pharmgkbrs794729366
gwascentralrs794729366
openSNPrs794729366
23andMers794729366
23andMe allrs794729366
SNP Nexus

SNPshotrs794729366
SNPdbers794729366
MSV3drs794729366
GWAS Ctlgrs794729366
Max Magnitude0
ClinVar
Risk rs794729366(A;A)
Alt rs794729366(A;A)
Reference rs794729366(TTT;TTT)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179406270_179406272delAAAinsT
CLNSRC
CLNACC RCV000184365.1,