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rs794729281

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729281(C;T)
Make rs794729281(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178577085
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729281
ebirs794729281
HLIrs794729281
Exacrs794729281
Varsomers794729281
Maprs794729281
PheGenIrs794729281
hapmaprs794729281
1000 genomesrs794729281
hgdprs794729281
ensemblrs794729281
gopubmedrs794729281
geneviewrs794729281
scholarrs794729281
googlers794729281
pharmgkbrs794729281
gwascentralrs794729281
openSNPrs794729281
23andMers794729281
23andMe allrs794729281
SNP Nexus

SNPshotrs794729281
SNPdbers794729281
MSV3drs794729281
GWAS Ctlgrs794729281
Max Magnitude0
ClinVar
Risk rs794729281(T;T)
Alt rs794729281(T;T)
Reference rs794729281(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179441812G>A
CLNSRC
CLNACC RCV000184254.1,