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rs794729295

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729295(G;T)
Make rs794729295(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178562479
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729295
ebirs794729295
HLIrs794729295
Exacrs794729295
Varsomers794729295
Maprs794729295
PheGenIrs794729295
hapmaprs794729295
1000 genomesrs794729295
hgdprs794729295
ensemblrs794729295
gopubmedrs794729295
geneviewrs794729295
scholarrs794729295
googlers794729295
pharmgkbrs794729295
gwascentralrs794729295
openSNPrs794729295
23andMers794729295
23andMe allrs794729295
SNP Nexus

SNPshotrs794729295
SNPdbers794729295
MSV3drs794729295
GWAS Ctlgrs794729295
Max Magnitude0
ClinVar
Risk rs794729295(T;T)
Alt rs794729295(T;T)
Reference rs794729295(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179427206C>A
CLNSRC
CLNACC RCV000184274.1,