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rs794729284

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729284(C;T)
Make rs794729284(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178572286
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729284
ebirs794729284
HLIrs794729284
Exacrs794729284
Varsomers794729284
Maprs794729284
PheGenIrs794729284
hapmaprs794729284
1000 genomesrs794729284
hgdprs794729284
ensemblrs794729284
gopubmedrs794729284
geneviewrs794729284
scholarrs794729284
googlers794729284
pharmgkbrs794729284
gwascentralrs794729284
openSNPrs794729284
23andMers794729284
23andMe allrs794729284
SNP Nexus

SNPshotrs794729284
SNPdbers794729284
MSV3drs794729284
GWAS Ctlgrs794729284
Max Magnitude0
ClinVar
Risk rs794729284(T;T)
Alt rs794729284(T;T)
Reference rs794729284(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179437013G>A
CLNSRC
CLNACC RCV000184260.2,