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rs794729364

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729364(-;-)
Make rs794729364(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178544459
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729364
ebirs794729364
HLIrs794729364
Exacrs794729364
Varsomers794729364
Maprs794729364
PheGenIrs794729364
hapmaprs794729364
1000 genomesrs794729364
hgdprs794729364
ensemblrs794729364
gopubmedrs794729364
geneviewrs794729364
scholarrs794729364
googlers794729364
pharmgkbrs794729364
gwascentralrs794729364
openSNPrs794729364
23andMers794729364
23andMe allrs794729364
SNP Nexus

SNPshotrs794729364
SNPdbers794729364
MSV3drs794729364
GWAS Ctlgrs794729364
Max Magnitude0
ClinVar
Risk rs794729364(;)
Alt rs794729364(;)
Reference rs794729364(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179409186delG
CLNSRC
CLNACC RCV000184362.1,