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rs387906874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906874(C;T)
Make rs387906874(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position119669881
GeneBAG3
is asnp
is mentioned by
dbSNPrs387906874
dbSNP (classic)rs387906874
ClinGenrs387906874
ebirs387906874
HLIrs387906874
Exacrs387906874
Gnomadrs387906874
Varsomers387906874
LitVarrs387906874
Maprs387906874
PheGenIrs387906874
Biobankrs387906874
1000 genomesrs387906874
hgdprs387906874
ensemblrs387906874
geneviewrs387906874
scholarrs387906874
googlers387906874
pharmgkbrs387906874
gwascentralrs387906874
openSNPrs387906874
23andMers387906874
SNPshotrs387906874
SNPdbers387906874
MSV3drs387906874
GWAS Ctlgrs387906874
Max Magnitude0
ClinVar
Risk rs387906874(T;T)
Alt rs387906874(T;T)
Reference Rs387906874(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1HH Myofibrillar myopathy
Variation info
Gene BAG3
CLNDBN Dilated cardiomyopathy 1HH Myofibrillar myopathy, BAG3-related
Reversed 0
HGVS NC_000010.10:g.121429393C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000023349.2, RCV000456156.1,