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rs794729303

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729303(G;G)
Make rs794729303(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178543832
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729303
ebirs794729303
HLIrs794729303
Exacrs794729303
Varsomers794729303
Maprs794729303
PheGenIrs794729303
hapmaprs794729303
1000 genomesrs794729303
hgdprs794729303
ensemblrs794729303
gopubmedrs794729303
geneviewrs794729303
scholarrs794729303
googlers794729303
pharmgkbrs794729303
gwascentralrs794729303
openSNPrs794729303
23andMers794729303
23andMe allrs794729303
SNP Nexus

SNPshotrs794729303
SNPdbers794729303
MSV3drs794729303
GWAS Ctlgrs794729303
Max Magnitude0
ClinVar
Risk rs794729303(G;G)
Alt rs794729303(G;G)
Reference rs794729303(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179408559A>C
CLNSRC
CLNACC RCV000184283.2,