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rs202247821

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs202247821(-;-)
Make rs202247821(-;CCC)
Make rs202247821(CCC;CCC)
ReferenceGRCh38 38.1/141
Chromosome3
Position136329945
GenePCCB
is asnp
is mentioned by
dbSNPrs202247821
ebirs202247821
HLIrs202247821
Exacrs202247821
Varsomers202247821
Maprs202247821
PheGenIrs202247821
hapmaprs202247821
1000 genomesrs202247821
hgdprs202247821
ensemblrs202247821
gopubmedrs202247821
geneviewrs202247821
scholarrs202247821
googlers202247821
pharmgkbrs202247821
gwascentralrs202247821
openSNPrs202247821
23andMers202247821
23andMe allrs202247821
SNP Nexus

SNPshotrs202247821
SNPdbers202247821
MSV3drs202247821
GWAS Ctlgrs202247821
Max Magnitude0
ClinVar
Risk rs202247821(CCC;CCC)
Alt rs202247821(CCC;CCC)
Reference rs202247821(;)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136048787_136048788insCCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012797.22,