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rs794729362

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729362(-;-)
Make rs794729362(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178553736
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729362
ebirs794729362
HLIrs794729362
Exacrs794729362
Varsomers794729362
Maprs794729362
PheGenIrs794729362
hapmaprs794729362
1000 genomesrs794729362
hgdprs794729362
ensemblrs794729362
gopubmedrs794729362
geneviewrs794729362
scholarrs794729362
googlers794729362
pharmgkbrs794729362
gwascentralrs794729362
openSNPrs794729362
23andMers794729362
23andMe allrs794729362
SNP Nexus

SNPshotrs794729362
SNPdbers794729362
MSV3drs794729362
GWAS Ctlgrs794729362
Max Magnitude0
ClinVar
Risk rs794729362(;)
Alt rs794729362(;)
Reference rs794729362(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179418463delT
CLNSRC
CLNACC RCV000184355.1,