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rs794729342

From SNPedia

Orientationminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs794729342(-;-)
Make rs794729342(-;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178569734
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729342
ebirs794729342
HLIrs794729342
Exacrs794729342
Varsomers794729342
Maprs794729342
PheGenIrs794729342
hapmaprs794729342
1000 genomesrs794729342
hgdprs794729342
ensemblrs794729342
gopubmedrs794729342
geneviewrs794729342
scholarrs794729342
googlers794729342
pharmgkbrs794729342
gwascentralrs794729342
openSNPrs794729342
23andMers794729342
23andMe allrs794729342
SNP Nexus

SNPshotrs794729342
SNPdbers794729342
MSV3drs794729342
GWAS Ctlgrs794729342
Max Magnitude0
ClinVar
Risk rs794729342(;)
Alt rs794729342(;)
Reference rs794729342(TA;TA)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179434461_179434462delTA
CLNSRC
CLNACC RCV000184332.1,