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rs189768576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs189768576(A;A)
Make rs189768576(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97828127
GeneDPYD
is asnp
is mentioned by
dbSNPrs189768576
dbSNP (old)rs189768576
ClinGenrs189768576
ebirs189768576
HLIrs189768576
Exacrs189768576
Gnomadrs189768576
Varsomers189768576
LitVarrs189768576
Maprs189768576
PheGenIrs189768576
Biobankrs189768576
1000 genomesrs189768576
hgdprs189768576
ensemblrs189768576
gopubmedrs189768576
geneviewrs189768576
scholarrs189768576
googlers189768576
pharmgkbrs189768576
gwascentralrs189768576
openSNPrs189768576
23andMers189768576
23andMe allrs189768576
SNPshotrs189768576
SNPdbers189768576
MSV3drs189768576
GWAS Ctlgrs189768576
Max Magnitude0
ClinVar
Risk rs189768576(A;A)
Alt rs189768576(A;A)
Reference Rs189768576(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.98293683G>A
CLNSRC
CLNACC RCV000411323.1,