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rs121964960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964960(A;A)
Make rs121964960(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position136262024
GenePCCB
is asnp
is mentioned by
dbSNPrs121964960
ebirs121964960
HLIrs121964960
Exacrs121964960
Varsomers121964960
Maprs121964960
PheGenIrs121964960
hapmaprs121964960
1000 genomesrs121964960
hgdprs121964960
ensemblrs121964960
gopubmedrs121964960
geneviewrs121964960
scholarrs121964960
googlers121964960
pharmgkbrs121964960
gwascentralrs121964960
openSNPrs121964960
23andMers121964960
23andMe allrs121964960
SNP Nexus

SNPshotrs121964960
SNPdbers121964960
MSV3drs121964960
GWAS Ctlgrs121964960
Max Magnitude0
OMIM232050
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121964960(A;A)
Alt rs121964960(A;A)
Reference rs121964960(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135980866G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012795.22,