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rs794729350

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs794729350(A;A)
Make rs794729350(A;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178563415
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729350
ebirs794729350
HLIrs794729350
Exacrs794729350
Varsomers794729350
Maprs794729350
PheGenIrs794729350
hapmaprs794729350
1000 genomesrs794729350
hgdprs794729350
ensemblrs794729350
gopubmedrs794729350
geneviewrs794729350
scholarrs794729350
googlers794729350
pharmgkbrs794729350
gwascentralrs794729350
openSNPrs794729350
23andMers794729350
23andMe allrs794729350
SNP Nexus

SNPshotrs794729350
SNPdbers794729350
MSV3drs794729350
GWAS Ctlgrs794729350
Max Magnitude0
ClinVar
Risk rs794729350(A;A)
Alt rs794729350(A;A)
Reference rs794729350(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179428142_179428143delGAinsT
CLNSRC
CLNACC RCV000184343.1,