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rs794729328

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729328(-;-)
Make rs794729328(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178588204
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729328
ebirs794729328
HLIrs794729328
Exacrs794729328
Varsomers794729328
Maprs794729328
PheGenIrs794729328
hapmaprs794729328
1000 genomesrs794729328
hgdprs794729328
ensemblrs794729328
gopubmedrs794729328
geneviewrs794729328
scholarrs794729328
googlers794729328
pharmgkbrs794729328
gwascentralrs794729328
openSNPrs794729328
23andMers794729328
23andMe allrs794729328
SNP Nexus

SNPshotrs794729328
SNPdbers794729328
MSV3drs794729328
GWAS Ctlgrs794729328
Max Magnitude0
ClinVar
Risk rs794729328(;)
Alt rs794729328(;)
Reference rs794729328(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179452931delG
CLNSRC
CLNACC RCV000184317.1,