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rs794729273

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729273(A;A)
Make rs794729273(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178607247
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729273
ebirs794729273
HLIrs794729273
Exacrs794729273
Varsomers794729273
Maprs794729273
PheGenIrs794729273
hapmaprs794729273
1000 genomesrs794729273
hgdprs794729273
ensemblrs794729273
gopubmedrs794729273
geneviewrs794729273
scholarrs794729273
googlers794729273
pharmgkbrs794729273
gwascentralrs794729273
openSNPrs794729273
23andMers794729273
23andMe allrs794729273
SNP Nexus

SNPshotrs794729273
SNPdbers794729273
MSV3drs794729273
GWAS Ctlgrs794729273
Max Magnitude0
ClinVar
Risk rs794729273(A;A)
Alt rs794729273(A;A)
Reference rs794729273(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179471974C>T
CLNSRC
CLNACC RCV000184236.1,