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rs794729396

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794729396(-;-)
Make rs794729396(-;GG)
Make rs794729396(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178538643
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729396
ebirs794729396
HLIrs794729396
Exacrs794729396
Varsomers794729396
Maprs794729396
PheGenIrs794729396
hapmaprs794729396
1000 genomesrs794729396
hgdprs794729396
ensemblrs794729396
gopubmedrs794729396
geneviewrs794729396
scholarrs794729396
googlers794729396
pharmgkbrs794729396
gwascentralrs794729396
openSNPrs794729396
23andMers794729396
23andMe allrs794729396
SNP Nexus

SNPshotrs794729396
SNPdbers794729396
MSV3drs794729396
GWAS Ctlgrs794729396
Max Magnitude0
ClinVar
Risk rs794729396(GG;GG)
Alt rs794729396(GG;GG)
Reference rs794729396(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179403371_179403372dupCC
CLNSRC
CLNACC RCV000184413.1,