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rs794729322

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729322(-;-)
Make rs794729322(-;AACT)
Make rs794729322(AACT;AACT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178611877
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729322
ebirs794729322
HLIrs794729322
Exacrs794729322
Varsomers794729322
Maprs794729322
PheGenIrs794729322
hapmaprs794729322
1000 genomesrs794729322
hgdprs794729322
ensemblrs794729322
gopubmedrs794729322
geneviewrs794729322
scholarrs794729322
googlers794729322
pharmgkbrs794729322
gwascentralrs794729322
openSNPrs794729322
23andMers794729322
23andMe allrs794729322
SNP Nexus

SNPshotrs794729322
SNPdbers794729322
MSV3drs794729322
GWAS Ctlgrs794729322
Max Magnitude0
ClinVar
Risk rs794729322(AACT;AACT)
Alt rs794729322(AACT;AACT)
Reference rs794729322(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179476605_179476608dupAGTT
CLNSRC
CLNACC RCV000184310.1,