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rs794727092

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727092(G;T)
Make rs794727092(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136327733
GenePCCB
is asnp
is mentioned by
dbSNPrs794727092
ebirs794727092
HLIrs794727092
Exacrs794727092
Varsomers794727092
Maprs794727092
PheGenIrs794727092
hapmaprs794727092
1000 genomesrs794727092
hgdprs794727092
ensemblrs794727092
gopubmedrs794727092
geneviewrs794727092
scholarrs794727092
googlers794727092
pharmgkbrs794727092
gwascentralrs794727092
openSNPrs794727092
23andMers794727092
23andMe allrs794727092
SNP Nexus

SNPshotrs794727092
SNPdbers794727092
MSV3drs794727092
GWAS Ctlgrs794727092
Max Magnitude0
ClinVar
Risk rs794727092(T;T)
Alt rs794727092(T;T)
Reference rs794727092(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.136046575G>T
CLNSRC
CLNACC RCV000174489.1,