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rs387906875

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906875(C;T)
Make rs387906875(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position119670037
GeneBAG3
is asnp
is mentioned by
dbSNPrs387906875
dbSNP (classic)rs387906875
ClinGenrs387906875
ebirs387906875
HLIrs387906875
Exacrs387906875
Gnomadrs387906875
Varsomers387906875
LitVarrs387906875
Maprs387906875
PheGenIrs387906875
Biobankrs387906875
1000 genomesrs387906875
hgdprs387906875
ensemblrs387906875
geneviewrs387906875
scholarrs387906875
googlers387906875
pharmgkbrs387906875
gwascentralrs387906875
openSNPrs387906875
23andMers387906875
SNPshotrs387906875
SNPdbers387906875
MSV3drs387906875
GWAS Ctlgrs387906875
Max Magnitude0
ClinVar
Risk rs387906875(T;T)
Alt rs387906875(T;T)
Reference Rs387906875(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1HH Primary dilated cardiomyopathy Cardiovascular phenotype not provided
Variation info
Gene BAG3
CLNDBN Dilated cardiomyopathy 1HH Primary dilated cardiomyopathy Cardiovascular phenotype not provided
Reversed 0
HGVS NC_000010.10:g.121429549C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023350.4, RCV000211711.1, RCV000247382.1, RCV000254992.2,