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rs794729338

From SNPedia

Orientationminus
Geno Mag Summary
(GCATATG;GCATATG) 0 common in clinvar
Make rs794729338(GCATATG;TA)
Make rs794729338(TA;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178574146
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729338
ebirs794729338
HLIrs794729338
Exacrs794729338
Varsomers794729338
Maprs794729338
PheGenIrs794729338
hapmaprs794729338
1000 genomesrs794729338
hgdprs794729338
ensemblrs794729338
gopubmedrs794729338
geneviewrs794729338
scholarrs794729338
googlers794729338
pharmgkbrs794729338
gwascentralrs794729338
openSNPrs794729338
23andMers794729338
23andMe allrs794729338
SNP Nexus

SNPshotrs794729338
SNPdbers794729338
MSV3drs794729338
GWAS Ctlgrs794729338
Max Magnitude0
ClinVar
Risk rs794729338(TA;TA)
Alt rs794729338(TA;TA)
Reference rs794729338(GCATATG;GCATATG)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179438873_179438879delCATATGCinsTA
CLNSRC
CLNACC RCV000184327.1,