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rs794729326

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729326(-;-)
Make rs794729326(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178601766
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729326
ebirs794729326
HLIrs794729326
Exacrs794729326
Varsomers794729326
Maprs794729326
PheGenIrs794729326
hapmaprs794729326
1000 genomesrs794729326
hgdprs794729326
ensemblrs794729326
gopubmedrs794729326
geneviewrs794729326
scholarrs794729326
googlers794729326
pharmgkbrs794729326
gwascentralrs794729326
openSNPrs794729326
23andMers794729326
23andMe allrs794729326
SNP Nexus

SNPshotrs794729326
SNPdbers794729326
MSV3drs794729326
GWAS Ctlgrs794729326
Max Magnitude0
ClinVar
Risk rs794729326(;)
Alt rs794729326(;)
Reference rs794729326(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179466493delA
CLNSRC
CLNACC RCV000184314.1,