Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729298

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729298(C;G)
Make rs794729298(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178559492
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729298
ebirs794729298
HLIrs794729298
Exacrs794729298
Varsomers794729298
Maprs794729298
PheGenIrs794729298
hapmaprs794729298
1000 genomesrs794729298
hgdprs794729298
ensemblrs794729298
gopubmedrs794729298
geneviewrs794729298
scholarrs794729298
googlers794729298
pharmgkbrs794729298
gwascentralrs794729298
openSNPrs794729298
23andMers794729298
23andMe allrs794729298
SNP Nexus

SNPshotrs794729298
SNPdbers794729298
MSV3drs794729298
GWAS Ctlgrs794729298
Max Magnitude0
ClinVar
Risk rs794729298(G;G)
Alt rs794729298(G;G)
Reference rs794729298(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179424219G>C
CLNSRC
CLNACC RCV000184277.2,