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rs794729262

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729262(A;A)
Make rs794729262(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178614297
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729262
ebirs794729262
HLIrs794729262
Exacrs794729262
Varsomers794729262
Maprs794729262
PheGenIrs794729262
hapmaprs794729262
1000 genomesrs794729262
hgdprs794729262
ensemblrs794729262
gopubmedrs794729262
geneviewrs794729262
scholarrs794729262
googlers794729262
pharmgkbrs794729262
gwascentralrs794729262
openSNPrs794729262
23andMers794729262
23andMe allrs794729262
SNP Nexus

SNPshotrs794729262
SNPdbers794729262
MSV3drs794729262
GWAS Ctlgrs794729262
Max Magnitude0
ClinVar
Risk rs794729262(A;A)
Alt rs794729262(A;A)
Reference rs794729262(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179479024G>T
CLNSRC
CLNACC RCV000184220.1,