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rs786205466

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205466(C;C)
Make rs786205466(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position119677184
GeneBAG3
is asnp
is mentioned by
dbSNPrs786205466
ebirs786205466
HLIrs786205466
Exacrs786205466
Varsomers786205466
Maprs786205466
PheGenIrs786205466
hapmaprs786205466
1000 genomesrs786205466
hgdprs786205466
ensemblrs786205466
gopubmedrs786205466
geneviewrs786205466
scholarrs786205466
googlers786205466
pharmgkbrs786205466
gwascentralrs786205466
openSNPrs786205466
23andMers786205466
23andMe allrs786205466
SNP Nexus

SNPshotrs786205466
SNPdbers786205466
MSV3drs786205466
GWAS Ctlgrs786205466
Max Magnitude0
ClinVar
Risk rs786205466(C;C)
Alt rs786205466(C;C)
Reference rs786205466(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BAG3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.121436696G>C
CLNSRC
CLNACC RCV000171190.1,