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rs794729311

From SNPedia

Orientationminus
Geno Mag Summary
(AACTAC;AACTAC) 0 common in clinvar
Make rs794729311(AACTAC;T)
Make rs794729311(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178790745
GeneTTN
is asnp
is mentioned by
dbSNPrs794729311
ebirs794729311
HLIrs794729311
Exacrs794729311
Varsomers794729311
Maprs794729311
PheGenIrs794729311
hapmaprs794729311
1000 genomesrs794729311
hgdprs794729311
ensemblrs794729311
gopubmedrs794729311
geneviewrs794729311
scholarrs794729311
googlers794729311
pharmgkbrs794729311
gwascentralrs794729311
openSNPrs794729311
23andMers794729311
23andMe allrs794729311
SNP Nexus

SNPshotrs794729311
SNPdbers794729311
MSV3drs794729311
GWAS Ctlgrs794729311
Max Magnitude0
ClinVar
Risk rs794729311(T;T)
Alt rs794729311(T;T)
Reference rs794729311(AACTAC;AACTAC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179655472_179655477delGTAGTTinsA
CLNSRC
CLNACC RCV000184296.1,