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rs876657373

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657373(A;G)
Make rs876657373(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position24523617
GeneUPB1
is asnp
is mentioned by
dbSNPrs876657373
ebirs876657373
HLIrs876657373
Exacrs876657373
Varsomers876657373
Maprs876657373
PheGenIrs876657373
hapmaprs876657373
1000 genomesrs876657373
hgdprs876657373
ensemblrs876657373
gopubmedrs876657373
geneviewrs876657373
scholarrs876657373
googlers876657373
pharmgkbrs876657373
gwascentralrs876657373
openSNPrs876657373
23andMers876657373
23andMe allrs876657373
SNP Nexus

SNPshotrs876657373
SNPdbers876657373
MSV3drs876657373
GWAS Ctlgrs876657373
Max Magnitude0
ClinVar
Risk rs876657373(G;G)
Alt rs876657373(G;G)
Reference rs876657373(A;A)
Significance Pathogenic
Disease Deficiency of beta-ureidopropionase
Variation info
Gene UPB1
CLNDBN Deficiency of beta-ureidopropionase
Reversed 0
HGVS NC_000022.10:g.24919585A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004364.3,