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rs794729361

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729361(-;-)
Make rs794729361(-;T)
Make rs794729361(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178554104
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729361
ebirs794729361
HLIrs794729361
Exacrs794729361
Varsomers794729361
Maprs794729361
PheGenIrs794729361
hapmaprs794729361
1000 genomesrs794729361
hgdprs794729361
ensemblrs794729361
gopubmedrs794729361
geneviewrs794729361
scholarrs794729361
googlers794729361
pharmgkbrs794729361
gwascentralrs794729361
openSNPrs794729361
23andMers794729361
23andMe allrs794729361
SNP Nexus

SNPshotrs794729361
SNPdbers794729361
MSV3drs794729361
GWAS Ctlgrs794729361
Max Magnitude0
ClinVar
Risk rs794729361(T;T)
Alt rs794729361(T;T)
Reference rs794729361(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179418832dupA
CLNSRC
CLNACC RCV000184354.1,