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rs794729341

From SNPedia

Orientationminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs794729341(AGGG;AGGG)
Make rs794729341(AGGG;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178569974
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs794729341
ebirs794729341
HLIrs794729341
Exacrs794729341
Varsomers794729341
Maprs794729341
PheGenIrs794729341
hapmaprs794729341
1000 genomesrs794729341
hgdprs794729341
ensemblrs794729341
gopubmedrs794729341
geneviewrs794729341
scholarrs794729341
googlers794729341
pharmgkbrs794729341
gwascentralrs794729341
openSNPrs794729341
23andMers794729341
23andMe allrs794729341
SNP Nexus

SNPshotrs794729341
SNPdbers794729341
MSV3drs794729341
GWAS Ctlgrs794729341
Max Magnitude0
ClinVar
Risk rs794729341(AGGG;AGGG)
Alt rs794729341(AGGG;AGGG)
Reference rs794729341(GA;GA)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179434701_179434702delTCinsCCCT
CLNSRC
CLNACC RCV000184331.1,