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rs794729283

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729283(A;A)
Make rs794729283(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178572947
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729283
ClinGenrs794729283
ebirs794729283
HLIrs794729283
Exacrs794729283
Varsomers794729283
Maprs794729283
PheGenIrs794729283
hapmaprs794729283
1000 genomesrs794729283
hgdprs794729283
ensemblrs794729283
gopubmedrs794729283
geneviewrs794729283
scholarrs794729283
googlers794729283
pharmgkbrs794729283
gwascentralrs794729283
openSNPrs794729283
23andMers794729283
23andMe allrs794729283
SNP Nexus

SNPshotrs794729283
SNPdbers794729283
MSV3drs794729283
GWAS Ctlgrs794729283
Max Magnitude0
ClinVar
Risk rs794729283(A;A)
Alt rs794729283(A;A)
Reference Rs794729283(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179437674A>T
CLNSRC
CLNACC RCV000184259.1,