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rs794729394

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729394(-;-)
Make rs794729394(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178564930
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729394
ebirs794729394
HLIrs794729394
Exacrs794729394
Varsomers794729394
Maprs794729394
PheGenIrs794729394
hapmaprs794729394
1000 genomesrs794729394
hgdprs794729394
ensemblrs794729394
gopubmedrs794729394
geneviewrs794729394
scholarrs794729394
googlers794729394
pharmgkbrs794729394
gwascentralrs794729394
openSNPrs794729394
23andMers794729394
23andMe allrs794729394
SNP Nexus

SNPshotrs794729394
SNPdbers794729394
MSV3drs794729394
GWAS Ctlgrs794729394
Max Magnitude0
ClinVar
Risk rs794729394(;)
Alt rs794729394(;)
Reference rs794729394(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179429657delA
CLNSRC
CLNACC RCV000184411.1,