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rs794729367

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729367(CT;CT)
Make rs794729367(CT;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178535517
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729367
ebirs794729367
HLIrs794729367
Exacrs794729367
Varsomers794729367
Maprs794729367
PheGenIrs794729367
hapmaprs794729367
1000 genomesrs794729367
hgdprs794729367
ensemblrs794729367
gopubmedrs794729367
geneviewrs794729367
scholarrs794729367
googlers794729367
pharmgkbrs794729367
gwascentralrs794729367
openSNPrs794729367
23andMers794729367
23andMe allrs794729367
SNP Nexus

SNPshotrs794729367
SNPdbers794729367
MSV3drs794729367
GWAS Ctlgrs794729367
Max Magnitude0
ClinVar
Risk rs794729367(CT;CT)
Alt rs794729367(CT;CT)
Reference rs794729367(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179400244delCinsAG
CLNSRC
CLNACC RCV000184366.1,