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rs794729360

From SNPedia

Orientationminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs794729360(-;-)
Make rs794729360(-;AC)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178554643
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729360
ebirs794729360
HLIrs794729360
Exacrs794729360
Varsomers794729360
Maprs794729360
PheGenIrs794729360
hapmaprs794729360
1000 genomesrs794729360
hgdprs794729360
ensemblrs794729360
gopubmedrs794729360
geneviewrs794729360
scholarrs794729360
googlers794729360
pharmgkbrs794729360
gwascentralrs794729360
openSNPrs794729360
23andMers794729360
23andMe allrs794729360
SNP Nexus

SNPshotrs794729360
SNPdbers794729360
MSV3drs794729360
GWAS Ctlgrs794729360
Max Magnitude0
ClinVar
Risk rs794729360(;)
Alt rs794729360(;)
Reference rs794729360(AC;AC)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179419370_179419371delGT
CLNSRC
CLNACC RCV000184353.1,