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rs794729331

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729331(-;-)
Make rs794729331(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178583651
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729331
ebirs794729331
HLIrs794729331
Exacrs794729331
Varsomers794729331
Maprs794729331
PheGenIrs794729331
hapmaprs794729331
1000 genomesrs794729331
hgdprs794729331
ensemblrs794729331
gopubmedrs794729331
geneviewrs794729331
scholarrs794729331
googlers794729331
pharmgkbrs794729331
gwascentralrs794729331
openSNPrs794729331
23andMers794729331
23andMe allrs794729331
SNP Nexus

SNPshotrs794729331
SNPdbers794729331
MSV3drs794729331
GWAS Ctlgrs794729331
Max Magnitude0
ClinVar
Risk rs794729331(;)
Alt rs794729331(;)
Reference rs794729331(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179448378delG
CLNSRC
CLNACC RCV000184320.1,