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rs794729288

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729288(C;T)
Make rs794729288(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178568368
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729288
ebirs794729288
HLIrs794729288
Exacrs794729288
Varsomers794729288
Maprs794729288
PheGenIrs794729288
hapmaprs794729288
1000 genomesrs794729288
hgdprs794729288
ensemblrs794729288
gopubmedrs794729288
geneviewrs794729288
scholarrs794729288
googlers794729288
pharmgkbrs794729288
gwascentralrs794729288
openSNPrs794729288
23andMers794729288
23andMe allrs794729288
SNP Nexus

SNPshotrs794729288
SNPdbers794729288
MSV3drs794729288
GWAS Ctlgrs794729288
Max Magnitude0
ClinVar
Risk rs794729288(T;T)
Alt rs794729288(T;T)
Reference rs794729288(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179433095G>A
CLNSRC
CLNACC RCV000184264.1,