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rs794729335

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729335(-;-)
Make rs794729335(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178575300
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729335
ebirs794729335
HLIrs794729335
Exacrs794729335
Varsomers794729335
Maprs794729335
PheGenIrs794729335
hapmaprs794729335
1000 genomesrs794729335
hgdprs794729335
ensemblrs794729335
gopubmedrs794729335
geneviewrs794729335
scholarrs794729335
googlers794729335
pharmgkbrs794729335
gwascentralrs794729335
openSNPrs794729335
23andMers794729335
23andMe allrs794729335
SNP Nexus

SNPshotrs794729335
SNPdbers794729335
MSV3drs794729335
GWAS Ctlgrs794729335
Max Magnitude0
ClinVar
Risk rs794729335(;)
Alt rs794729335(;)
Reference rs794729335(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179440027delG
CLNSRC
CLNACC RCV000184324.2,