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rs794729282

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729282(G;T)
Make rs794729282(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178576417
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729282
ebirs794729282
HLIrs794729282
Exacrs794729282
Varsomers794729282
Maprs794729282
PheGenIrs794729282
hapmaprs794729282
1000 genomesrs794729282
hgdprs794729282
ensemblrs794729282
gopubmedrs794729282
geneviewrs794729282
scholarrs794729282
googlers794729282
pharmgkbrs794729282
gwascentralrs794729282
openSNPrs794729282
23andMers794729282
23andMe allrs794729282
SNP Nexus

SNPshotrs794729282
SNPdbers794729282
MSV3drs794729282
GWAS Ctlgrs794729282
Max Magnitude0
ClinVar
Risk rs794729282(T;T)
Alt rs794729282(T;T)
Reference rs794729282(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179441144C>A
CLNSRC
CLNACC RCV000184255.1,