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rs794729261

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729261(C;T)
Make rs794729261(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178617872
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729261
ebirs794729261
HLIrs794729261
Exacrs794729261
Varsomers794729261
Maprs794729261
PheGenIrs794729261
hapmaprs794729261
1000 genomesrs794729261
hgdprs794729261
ensemblrs794729261
gopubmedrs794729261
geneviewrs794729261
scholarrs794729261
googlers794729261
pharmgkbrs794729261
gwascentralrs794729261
openSNPrs794729261
23andMers794729261
23andMe allrs794729261
SNP Nexus

SNPshotrs794729261
SNPdbers794729261
MSV3drs794729261
GWAS Ctlgrs794729261
Max Magnitude0
ClinVar
Risk rs794729261(T;T)
Alt rs794729261(T;T)
Reference rs794729261(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179482599G>A
CLNSRC
CLNACC RCV000184217.2,