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rs886039044

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039044(C;T)
Make rs886039044(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position119670151
GeneBAG3
is asnp
is mentioned by
dbSNPrs886039044
dbSNP (classic)rs886039044
ClinGenrs886039044
ebirs886039044
HLIrs886039044
Exacrs886039044
Gnomadrs886039044
Varsomers886039044
LitVarrs886039044
Maprs886039044
PheGenIrs886039044
Biobankrs886039044
1000 genomesrs886039044
hgdprs886039044
ensemblrs886039044
geneviewrs886039044
scholarrs886039044
googlers886039044
pharmgkbrs886039044
gwascentralrs886039044
openSNPrs886039044
23andMers886039044
23andMe allrs886039044
SNPshotrs886039044
SNPdbers886039044
MSV3drs886039044
GWAS Ctlgrs886039044
Max Magnitude0
ClinVar
Risk rs886039044(T;T)
Alt rs886039044(T;T)
Reference Rs886039044(C;C)
Significance Pathogenic
Disease Cardiovascular phenotype
Variation info
Gene BAG3
CLNDBN Cardiovascular phenotype
Reversed 0
HGVS NC_000010.10:g.121429663C>T
CLNSRC
CLNACC RCV000244257.1,