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rs794729263

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729263(A;T)
Make rs794729263(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178613939
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729263
ebirs794729263
HLIrs794729263
Exacrs794729263
Varsomers794729263
Maprs794729263
PheGenIrs794729263
hapmaprs794729263
1000 genomesrs794729263
hgdprs794729263
ensemblrs794729263
gopubmedrs794729263
geneviewrs794729263
scholarrs794729263
googlers794729263
pharmgkbrs794729263
gwascentralrs794729263
openSNPrs794729263
23andMers794729263
23andMe allrs794729263
SNP Nexus

SNPshotrs794729263
SNPdbers794729263
MSV3drs794729263
GWAS Ctlgrs794729263
Max Magnitude0
ClinVar
Risk rs794729263(T;T)
Alt rs794729263(T;T)
Reference rs794729263(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179478666T>A
CLNSRC
CLNACC RCV000184221.1,