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rs794729332

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794729332(-;-)
Make rs794729332(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178579776
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729332
ebirs794729332
HLIrs794729332
Exacrs794729332
Varsomers794729332
Maprs794729332
PheGenIrs794729332
hapmaprs794729332
1000 genomesrs794729332
hgdprs794729332
ensemblrs794729332
gopubmedrs794729332
geneviewrs794729332
scholarrs794729332
googlers794729332
pharmgkbrs794729332
gwascentralrs794729332
openSNPrs794729332
23andMers794729332
23andMe allrs794729332
SNP Nexus

SNPshotrs794729332
SNPdbers794729332
MSV3drs794729332
GWAS Ctlgrs794729332
Max Magnitude0
ClinVar
Risk rs794729332(;)
Alt rs794729332(;)
Reference rs794729332(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179444503delT
CLNSRC
CLNACC RCV000184321.1,