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rs794729382

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729382(C;T)
Make rs794729382(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178570804
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729382
ebirs794729382
HLIrs794729382
Exacrs794729382
Varsomers794729382
Maprs794729382
PheGenIrs794729382
hapmaprs794729382
1000 genomesrs794729382
hgdprs794729382
ensemblrs794729382
gopubmedrs794729382
geneviewrs794729382
scholarrs794729382
googlers794729382
pharmgkbrs794729382
gwascentralrs794729382
openSNPrs794729382
23andMers794729382
23andMe allrs794729382
SNP Nexus

SNPshotrs794729382
SNPdbers794729382
MSV3drs794729382
GWAS Ctlgrs794729382
Max Magnitude0
ClinVar
Risk rs794729382(T;T)
Alt rs794729382(T;T)
Reference rs794729382(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179435531G>A
CLNSRC
CLNACC RCV000184390.1,