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rs794729363

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs794729363(-;-)
Make rs794729363(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178552246
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729363
ebirs794729363
HLIrs794729363
Exacrs794729363
Varsomers794729363
Maprs794729363
PheGenIrs794729363
hapmaprs794729363
1000 genomesrs794729363
hgdprs794729363
ensemblrs794729363
gopubmedrs794729363
geneviewrs794729363
scholarrs794729363
googlers794729363
pharmgkbrs794729363
gwascentralrs794729363
openSNPrs794729363
23andMers794729363
23andMe allrs794729363
SNP Nexus

SNPshotrs794729363
SNPdbers794729363
MSV3drs794729363
GWAS Ctlgrs794729363
Max Magnitude0
ClinVar
Risk rs794729363(;)
Alt rs794729363(;)
Reference rs794729363(CA;CA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179416973_179416974delTG
CLNSRC
CLNACC RCV000184356.1,