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rs886039182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886039182(-;A)
Make rs886039182(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position119676846
GeneBAG3
is asnp
is mentioned by
dbSNPrs886039182
dbSNP (classic)rs886039182
ClinGenrs886039182
ebirs886039182
HLIrs886039182
Exacrs886039182
Gnomadrs886039182
Varsomers886039182
LitVarrs886039182
Maprs886039182
PheGenIrs886039182
Biobankrs886039182
1000 genomesrs886039182
hgdprs886039182
ensemblrs886039182
geneviewrs886039182
scholarrs886039182
googlers886039182
pharmgkbrs886039182
gwascentralrs886039182
openSNPrs886039182
23andMers886039182
23andMe allrs886039182
SNPshotrs886039182
SNPdbers886039182
MSV3drs886039182
GWAS Ctlgrs886039182
Max Magnitude0
ClinVar
Risk rs886039182(A;A)
Alt rs886039182(A;A)
Reference Rs886039182(-;-)
Significance Pathogenic
Disease Cardiovascular phenotype
Variation info
Gene BAG3
CLNDBN Cardiovascular phenotype
Reversed 0
HGVS NC_000010.10:g.121436358dupA
CLNSRC
CLNACC RCV000252646.1,