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rs794729272

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729272(C;T)
Make rs794729272(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178607788
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729272
ebirs794729272
HLIrs794729272
Exacrs794729272
Varsomers794729272
Maprs794729272
PheGenIrs794729272
hapmaprs794729272
1000 genomesrs794729272
hgdprs794729272
ensemblrs794729272
gopubmedrs794729272
geneviewrs794729272
scholarrs794729272
googlers794729272
pharmgkbrs794729272
gwascentralrs794729272
openSNPrs794729272
23andMers794729272
23andMe allrs794729272
SNP Nexus

SNPshotrs794729272
SNPdbers794729272
MSV3drs794729272
GWAS Ctlgrs794729272
Max Magnitude0
ClinVar
Risk rs794729272(T;T)
Alt rs794729272(T;T)
Reference rs794729272(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179472515G>A
CLNSRC
CLNACC RCV000184235.2,