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rs876661342

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661342(A;A)
Make rs876661342(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position119672446
GeneBAG3
is asnp
is mentioned by
dbSNPrs876661342
ebirs876661342
HLIrs876661342
Exacrs876661342
Varsomers876661342
Maprs876661342
PheGenIrs876661342
hapmaprs876661342
1000 genomesrs876661342
hgdprs876661342
ensemblrs876661342
gopubmedrs876661342
geneviewrs876661342
scholarrs876661342
googlers876661342
pharmgkbrs876661342
gwascentralrs876661342
openSNPrs876661342
23andMers876661342
23andMe allrs876661342
SNP Nexus

SNPshotrs876661342
SNPdbers876661342
MSV3drs876661342
GWAS Ctlgrs876661342
Max Magnitude0
ClinVar
Risk rs876661342(A;A)
Alt rs876661342(A;A)
Reference rs876661342(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BAG3
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.121431958C>A
CLNSRC
CLNACC RCV000223884.1,