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rs186710233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs186710233(C;T)
Make rs186710233(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136329940
GenePCCB
is asnp
is mentioned by
dbSNPrs186710233
ebirs186710233
HLIrs186710233
Exacrs186710233
Varsomers186710233
Maprs186710233
PheGenIrs186710233
hapmaprs186710233
1000 genomesrs186710233
hgdprs186710233
ensemblrs186710233
gopubmedrs186710233
geneviewrs186710233
scholarrs186710233
googlers186710233
pharmgkbrs186710233
gwascentralrs186710233
openSNPrs186710233
23andMers186710233
23andMe allrs186710233
SNP Nexus

SNPshotrs186710233
SNPdbers186710233
MSV3drs186710233
GWAS Ctlgrs186710233
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs186710233(T;T)
Alt rs186710233(T;T)
Reference rs186710233(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136048782C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032128.1,