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rs794729347

From SNPedia

Orientationminus
Geno Mag Summary
(TGTT;TGTT) 0 common in clinvar
Make rs794729347(-;-)
Make rs794729347(-;TGTT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178566323
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729347
ebirs794729347
HLIrs794729347
Exacrs794729347
Varsomers794729347
Maprs794729347
PheGenIrs794729347
hapmaprs794729347
1000 genomesrs794729347
hgdprs794729347
ensemblrs794729347
gopubmedrs794729347
geneviewrs794729347
scholarrs794729347
googlers794729347
pharmgkbrs794729347
gwascentralrs794729347
openSNPrs794729347
23andMers794729347
23andMe allrs794729347
SNP Nexus

SNPshotrs794729347
SNPdbers794729347
MSV3drs794729347
GWAS Ctlgrs794729347
Max Magnitude0
ClinVar
Risk rs794729347(;)
Alt rs794729347(;)
Reference rs794729347(TGTT;TGTT)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179431050_179431053delAACA
CLNSRC
CLNACC RCV000184337.1,