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rs794729292

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729292(G;T)
Make rs794729292(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178564795
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729292
ebirs794729292
HLIrs794729292
Exacrs794729292
Varsomers794729292
Maprs794729292
PheGenIrs794729292
hapmaprs794729292
1000 genomesrs794729292
hgdprs794729292
ensemblrs794729292
gopubmedrs794729292
geneviewrs794729292
scholarrs794729292
googlers794729292
pharmgkbrs794729292
gwascentralrs794729292
openSNPrs794729292
23andMers794729292
23andMe allrs794729292
SNP Nexus

SNPshotrs794729292
SNPdbers794729292
MSV3drs794729292
GWAS Ctlgrs794729292
Max Magnitude0
ClinVar
Risk rs794729292(T;T)
Alt rs794729292(T;T)
Reference rs794729292(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179429522C>A
CLNSRC
CLNACC RCV000184269.2,