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rs794728981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTGAAAGTG;GCTGAAAGTG) 0 common in clinvar
Make rs794728981(-;-)
Make rs794728981(-;CTGAAAGTGG)
Make rs794728981(CTGAAAGTGG;CTGAAAGTGG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position119676821
GeneBAG3
is asnp
is mentioned by
dbSNPrs794728981
dbSNP (old)rs794728981
ClinGenrs794728981
ebirs794728981
HLIrs794728981
Exacrs794728981
Gnomadrs794728981
Varsomers794728981
Maprs794728981
PheGenIrs794728981
Biobankrs794728981
1000 genomesrs794728981
hgdprs794728981
ensemblrs794728981
gopubmedrs794728981
geneviewrs794728981
scholarrs794728981
googlers794728981
pharmgkbrs794728981
gwascentralrs794728981
openSNPrs794728981
23andMers794728981
23andMe allrs794728981
SNP Nexus

SNPshotrs794728981
SNPdbers794728981
MSV3drs794728981
GWAS Ctlgrs794728981
Max Magnitude0
ClinVar
Risk rs794728981(-;-)
Alt rs794728981(-;-)
Reference Rs794728981(GCTGAAAGTG;GCTGAAAGTG)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene BAG3
CLNDBN not provided Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.121436333_121436342delCTGAAAGTGG
CLNSRC
CLNACC RCV000183323.1, RCV000190668.1,