Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729286

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729286(C;T)
Make rs794729286(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178570882
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729286
ebirs794729286
HLIrs794729286
Exacrs794729286
Varsomers794729286
Maprs794729286
PheGenIrs794729286
hapmaprs794729286
1000 genomesrs794729286
hgdprs794729286
ensemblrs794729286
gopubmedrs794729286
geneviewrs794729286
scholarrs794729286
googlers794729286
pharmgkbrs794729286
gwascentralrs794729286
openSNPrs794729286
23andMers794729286
23andMe allrs794729286
SNP Nexus

SNPshotrs794729286
SNPdbers794729286
MSV3drs794729286
GWAS Ctlgrs794729286
Max Magnitude0
ClinVar
Risk rs794729286(T;T)
Alt rs794729286(T;T)
Reference rs794729286(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179435609G>A
CLNSRC
CLNACC RCV000184262.2,