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rs794729266

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729266(A;G)
Make rs794729266(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178611679
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729266
ebirs794729266
HLIrs794729266
Exacrs794729266
Varsomers794729266
Maprs794729266
PheGenIrs794729266
hapmaprs794729266
1000 genomesrs794729266
hgdprs794729266
ensemblrs794729266
gopubmedrs794729266
geneviewrs794729266
scholarrs794729266
googlers794729266
pharmgkbrs794729266
gwascentralrs794729266
openSNPrs794729266
23andMers794729266
23andMe allrs794729266
SNP Nexus

SNPshotrs794729266
SNPdbers794729266
MSV3drs794729266
GWAS Ctlgrs794729266
Max Magnitude0
ClinVar
Risk rs794729266(G;G)
Alt rs794729266(G;G)
Reference rs794729266(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179476406T>C
CLNSRC
CLNACC RCV000184227.2,