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rs794729349

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729349(-;-)
Make rs794729349(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178563474
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729349
ebirs794729349
HLIrs794729349
Exacrs794729349
Varsomers794729349
Maprs794729349
PheGenIrs794729349
hapmaprs794729349
1000 genomesrs794729349
hgdprs794729349
ensemblrs794729349
gopubmedrs794729349
geneviewrs794729349
scholarrs794729349
googlers794729349
pharmgkbrs794729349
gwascentralrs794729349
openSNPrs794729349
23andMers794729349
23andMe allrs794729349
SNP Nexus

SNPshotrs794729349
SNPdbers794729349
MSV3drs794729349
GWAS Ctlgrs794729349
Max Magnitude0
ClinVar
Risk rs794729349(;)
Alt rs794729349(;)
Reference rs794729349(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179428201delC
CLNSRC
CLNACC RCV000184342.1,