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rs587776758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776758(-;-)
Make rs587776758(-;T)
Make rs587776758(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position136326885
GenePCCB
is asnp
is mentioned by
dbSNPrs587776758
ebirs587776758
HLIrs587776758
Exacrs587776758
Varsomers587776758
Maprs587776758
PheGenIrs587776758
hapmaprs587776758
1000 genomesrs587776758
hgdprs587776758
ensemblrs587776758
gopubmedrs587776758
geneviewrs587776758
scholarrs587776758
googlers587776758
pharmgkbrs587776758
gwascentralrs587776758
openSNPrs587776758
23andMers587776758
23andMe allrs587776758
SNP Nexus

SNPshotrs587776758
SNPdbers587776758
MSV3drs587776758
GWAS Ctlgrs587776758
Max Magnitude0
ClinVar
Risk rs587776758(T;T)
Alt rs587776758(T;T)
Reference rs587776758(;)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136045727dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012794.16,