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rs794729365

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729365(-;-)
Make rs794729365(-;A)
Make rs794729365(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178542803
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729365
ebirs794729365
HLIrs794729365
Exacrs794729365
Varsomers794729365
Maprs794729365
PheGenIrs794729365
hapmaprs794729365
1000 genomesrs794729365
hgdprs794729365
ensemblrs794729365
gopubmedrs794729365
geneviewrs794729365
scholarrs794729365
googlers794729365
pharmgkbrs794729365
gwascentralrs794729365
openSNPrs794729365
23andMers794729365
23andMe allrs794729365
SNP Nexus

SNPshotrs794729365
SNPdbers794729365
MSV3drs794729365
GWAS Ctlgrs794729365
Max Magnitude0
ClinVar
Risk rs794729365(A;A)
Alt rs794729365(A;A)
Reference rs794729365(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179407531dupT
CLNSRC
CLNACC RCV000184363.1,