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rs794729392

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729392(-;-)
Make rs794729392(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178598857
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729392
ebirs794729392
HLIrs794729392
Exacrs794729392
Varsomers794729392
Maprs794729392
PheGenIrs794729392
hapmaprs794729392
1000 genomesrs794729392
hgdprs794729392
ensemblrs794729392
gopubmedrs794729392
geneviewrs794729392
scholarrs794729392
googlers794729392
pharmgkbrs794729392
gwascentralrs794729392
openSNPrs794729392
23andMers794729392
23andMe allrs794729392
SNP Nexus

SNPshotrs794729392
SNPdbers794729392
MSV3drs794729392
GWAS Ctlgrs794729392
Max Magnitude0
ClinVar
Risk rs794729392(;)
Alt rs794729392(;)
Reference rs794729392(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179463584delA
CLNSRC
CLNACC RCV000184409.1,