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rs794729276

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729276(G;T)
Make rs794729276(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178592652
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729276
ebirs794729276
HLIrs794729276
Exacrs794729276
Varsomers794729276
Maprs794729276
PheGenIrs794729276
hapmaprs794729276
1000 genomesrs794729276
hgdprs794729276
ensemblrs794729276
gopubmedrs794729276
geneviewrs794729276
scholarrs794729276
googlers794729276
pharmgkbrs794729276
gwascentralrs794729276
openSNPrs794729276
23andMers794729276
23andMe allrs794729276
SNP Nexus

SNPshotrs794729276
SNPdbers794729276
MSV3drs794729276
GWAS Ctlgrs794729276
Max Magnitude0
ClinVar
Risk rs794729276(T;T)
Alt rs794729276(T;T)
Reference rs794729276(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179457379C>A
CLNSRC
CLNACC RCV000184242.2,