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rs794729344

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729344(-;-)
Make rs794729344(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178568955
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729344
ebirs794729344
HLIrs794729344
Exacrs794729344
Varsomers794729344
Maprs794729344
PheGenIrs794729344
hapmaprs794729344
1000 genomesrs794729344
hgdprs794729344
ensemblrs794729344
gopubmedrs794729344
geneviewrs794729344
scholarrs794729344
googlers794729344
pharmgkbrs794729344
gwascentralrs794729344
openSNPrs794729344
23andMers794729344
23andMe allrs794729344
SNP Nexus

SNPshotrs794729344
SNPdbers794729344
MSV3drs794729344
GWAS Ctlgrs794729344
Max Magnitude0
ClinVar
Risk rs794729344(;)
Alt rs794729344(;)
Reference rs794729344(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179433682delC
CLNSRC
CLNACC RCV000184334.1,