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rs1057516763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516763(G;T)
Make rs1057516763(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97721509
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516763
dbSNP (classic)rs1057516763
ClinGenrs1057516763
ebirs1057516763
HLIrs1057516763
Exacrs1057516763
Gnomadrs1057516763
Varsomers1057516763
LitVarrs1057516763
Maprs1057516763
PheGenIrs1057516763
Biobankrs1057516763
1000 genomesrs1057516763
hgdprs1057516763
ensemblrs1057516763
geneviewrs1057516763
scholarrs1057516763
googlers1057516763
pharmgkbrs1057516763
gwascentralrs1057516763
openSNPrs1057516763
23andMers1057516763
23andMe allrs1057516763
SNPshotrs1057516763
SNPdbers1057516763
MSV3drs1057516763
GWAS Ctlgrs1057516763
Max Magnitude0
ClinVar
Risk rs1057516763(T;T)
Alt rs1057516763(T;T)
Reference Rs1057516763(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98187065C>A
CLNSRC
CLNACC RCV000410851.1,