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rs794729351

From SNPedia

Orientationminus
Geno Mag Summary
(TGCAAGTGCT;TGCAAGTGCT) 0 common in clinvar
Make rs794729351(-;-)
Make rs794729351(-;TGCAAGTGCT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178563059
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729351
ebirs794729351
HLIrs794729351
Exacrs794729351
Varsomers794729351
Maprs794729351
PheGenIrs794729351
hapmaprs794729351
1000 genomesrs794729351
hgdprs794729351
ensemblrs794729351
gopubmedrs794729351
geneviewrs794729351
scholarrs794729351
googlers794729351
pharmgkbrs794729351
gwascentralrs794729351
openSNPrs794729351
23andMers794729351
23andMe allrs794729351
SNP Nexus

SNPshotrs794729351
SNPdbers794729351
MSV3drs794729351
GWAS Ctlgrs794729351
Max Magnitude0
ClinVar
Risk rs794729351(;)
Alt rs794729351(;)
Reference rs794729351(TGCAAGTGCT;TGCAAGTGCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179427786_179427795delAGCACTTGCA
CLNSRC
CLNACC RCV000184344.1,