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rs794729384

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729384(C;T)
Make rs794729384(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178560016
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729384
ebirs794729384
HLIrs794729384
Exacrs794729384
Varsomers794729384
Maprs794729384
PheGenIrs794729384
hapmaprs794729384
1000 genomesrs794729384
hgdprs794729384
ensemblrs794729384
gopubmedrs794729384
geneviewrs794729384
scholarrs794729384
googlers794729384
pharmgkbrs794729384
gwascentralrs794729384
openSNPrs794729384
23andMers794729384
23andMe allrs794729384
SNP Nexus

SNPshotrs794729384
SNPdbers794729384
MSV3drs794729384
GWAS Ctlgrs794729384
Max Magnitude0
ClinVar
Risk rs794729384(T;T)
Alt rs794729384(T;T)
Reference rs794729384(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179424743G>A
CLNSRC
CLNACC RCV000184392.1,