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rs794729277

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729277(C;T)
Make rs794729277(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178591698
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729277
ebirs794729277
HLIrs794729277
Exacrs794729277
Varsomers794729277
Maprs794729277
PheGenIrs794729277
hapmaprs794729277
1000 genomesrs794729277
hgdprs794729277
ensemblrs794729277
gopubmedrs794729277
geneviewrs794729277
scholarrs794729277
googlers794729277
pharmgkbrs794729277
gwascentralrs794729277
openSNPrs794729277
23andMers794729277
23andMe allrs794729277
SNP Nexus

SNPshotrs794729277
SNPdbers794729277
MSV3drs794729277
GWAS Ctlgrs794729277
Max Magnitude0
ClinVar
Risk rs794729277(T;T)
Alt rs794729277(T;T)
Reference rs794729277(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179456425G>A
CLNSRC
CLNACC RCV000184245.1,