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rs794729296

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794729296(A;A)
Make rs794729296(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178561235
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729296
ebirs794729296
HLIrs794729296
Exacrs794729296
Varsomers794729296
Maprs794729296
PheGenIrs794729296
hapmaprs794729296
1000 genomesrs794729296
hgdprs794729296
ensemblrs794729296
gopubmedrs794729296
geneviewrs794729296
scholarrs794729296
googlers794729296
pharmgkbrs794729296
gwascentralrs794729296
openSNPrs794729296
23andMers794729296
23andMe allrs794729296
SNP Nexus

SNPshotrs794729296
SNPdbers794729296
MSV3drs794729296
GWAS Ctlgrs794729296
Max Magnitude0
ClinVar
Risk rs794729296(A;A)
Alt rs794729296(A;A)
Reference rs794729296(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179425962C>T
CLNSRC
CLNACC RCV000184275.2,