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rs794729293

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729293(A;T)
Make rs794729293(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178564168
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729293
ebirs794729293
HLIrs794729293
Exacrs794729293
Varsomers794729293
Maprs794729293
PheGenIrs794729293
hapmaprs794729293
1000 genomesrs794729293
hgdprs794729293
ensemblrs794729293
gopubmedrs794729293
geneviewrs794729293
scholarrs794729293
googlers794729293
pharmgkbrs794729293
gwascentralrs794729293
openSNPrs794729293
23andMers794729293
23andMe allrs794729293
SNP Nexus

SNPshotrs794729293
SNPdbers794729293
MSV3drs794729293
GWAS Ctlgrs794729293
Max Magnitude0
ClinVar
Risk rs794729293(T;T)
Alt rs794729293(T;T)
Reference rs794729293(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179428895T>A
CLNSRC
CLNACC RCV000184270.1,