Have questions? Visit https://www.reddit.com/r/SNPedia

rs121964961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964961(A;G)
Make rs121964961(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136327638
GenePCCB
is asnp
is mentioned by
dbSNPrs121964961
ebirs121964961
HLIrs121964961
Exacrs121964961
Varsomers121964961
Maprs121964961
PheGenIrs121964961
hapmaprs121964961
1000 genomesrs121964961
hgdprs121964961
ensemblrs121964961
gopubmedrs121964961
geneviewrs121964961
scholarrs121964961
googlers121964961
pharmgkbrs121964961
gwascentralrs121964961
openSNPrs121964961
23andMers121964961
23andMe allrs121964961
SNP Nexus

SNPshotrs121964961
SNPdbers121964961
MSV3drs121964961
GWAS Ctlgrs121964961
Max Magnitude0
OMIM232050
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121964961(G;G)
Alt rs121964961(G;G)
Reference rs121964961(A;A)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136046480A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012798.24,