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rs794729321

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729321(-;-)
Make rs794729321(-;GTCA)
Make rs794729321(GTCA;GTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178612387
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729321
ebirs794729321
HLIrs794729321
Exacrs794729321
Varsomers794729321
Maprs794729321
PheGenIrs794729321
hapmaprs794729321
1000 genomesrs794729321
hgdprs794729321
ensemblrs794729321
gopubmedrs794729321
geneviewrs794729321
scholarrs794729321
googlers794729321
pharmgkbrs794729321
gwascentralrs794729321
openSNPrs794729321
23andMers794729321
23andMe allrs794729321
SNP Nexus

SNPshotrs794729321
SNPdbers794729321
MSV3drs794729321
GWAS Ctlgrs794729321
Max Magnitude0
ClinVar
Risk rs794729321(GTCA;GTCA)
Alt rs794729321(GTCA;GTCA)
Reference rs794729321(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179477115_179477118dupTGAC
CLNSRC
CLNACC RCV000184309.1,