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rs794729358

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729358(-;-)
Make rs794729358(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178557442
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729358
ebirs794729358
HLIrs794729358
Exacrs794729358
Varsomers794729358
Maprs794729358
PheGenIrs794729358
hapmaprs794729358
1000 genomesrs794729358
hgdprs794729358
ensemblrs794729358
gopubmedrs794729358
geneviewrs794729358
scholarrs794729358
googlers794729358
pharmgkbrs794729358
gwascentralrs794729358
openSNPrs794729358
23andMers794729358
23andMe allrs794729358
SNP Nexus

SNPshotrs794729358
SNPdbers794729358
MSV3drs794729358
GWAS Ctlgrs794729358
Max Magnitude0
ClinVar
Risk rs794729358(;)
Alt rs794729358(;)
Reference rs794729358(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179422169delG
CLNSRC
CLNACC RCV000184351.1,