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rs121964959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964959(C;T)
Make rs121964959(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position136327184
GenePCCB
is asnp
is mentioned by
dbSNPrs121964959
ebirs121964959
HLIrs121964959
Exacrs121964959
Varsomers121964959
Maprs121964959
PheGenIrs121964959
hapmaprs121964959
1000 genomesrs121964959
hgdprs121964959
ensemblrs121964959
gopubmedrs121964959
geneviewrs121964959
scholarrs121964959
googlers121964959
pharmgkbrs121964959
gwascentralrs121964959
openSNPrs121964959
23andMers121964959
23andMe allrs121964959
SNP Nexus

SNPshotrs121964959
SNPdbers121964959
MSV3drs121964959
GWAS Ctlgrs121964959
Max Magnitude0
OMIM232050
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121964959(T;T)
Alt rs121964959(T;T)
Reference rs121964959(C;C)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136046026C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012791.22,