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rs777027944

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777027944(A;A)
Make rs777027944(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position136327166
GenePCCB
is asnp
is mentioned by
dbSNPrs777027944
ebirs777027944
HLIrs777027944
Exacrs777027944
Varsomers777027944
Maprs777027944
PheGenIrs777027944
hapmaprs777027944
1000 genomesrs777027944
hgdprs777027944
ensemblrs777027944
gopubmedrs777027944
geneviewrs777027944
scholarrs777027944
googlers777027944
pharmgkbrs777027944
gwascentralrs777027944
openSNPrs777027944
23andMers777027944
23andMe allrs777027944
SNP Nexus

SNPshotrs777027944
SNPdbers777027944
MSV3drs777027944
GWAS Ctlgrs777027944
Max Magnitude0
ClinVar
Risk rs777027944(A;A)
Alt rs777027944(A;A)
Reference rs777027944(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136046008G>A
CLNSRC
CLNACC RCV000235547.1,