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rs794729274

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729274(A;A)
Make rs794729274(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178604127
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729274
ebirs794729274
HLIrs794729274
Exacrs794729274
Varsomers794729274
Maprs794729274
PheGenIrs794729274
hapmaprs794729274
1000 genomesrs794729274
hgdprs794729274
ensemblrs794729274
gopubmedrs794729274
geneviewrs794729274
scholarrs794729274
googlers794729274
pharmgkbrs794729274
gwascentralrs794729274
openSNPrs794729274
23andMers794729274
23andMe allrs794729274
SNP Nexus

SNPshotrs794729274
SNPdbers794729274
MSV3drs794729274
GWAS Ctlgrs794729274
Max Magnitude0
ClinVar
Risk rs794729274(A;A)
Alt rs794729274(A;A)
Reference rs794729274(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179468854C>T
CLNSRC
CLNACC RCV000184238.1,