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rs1057516713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516713(A;G)
Make rs1057516713(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97549746
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516713
dbSNP (old)rs1057516713
ClinGenrs1057516713
ebirs1057516713
HLIrs1057516713
Exacrs1057516713
Gnomadrs1057516713
Varsomers1057516713
LitVarrs1057516713
Maprs1057516713
PheGenIrs1057516713
Biobankrs1057516713
1000 genomesrs1057516713
hgdprs1057516713
ensemblrs1057516713
gopubmedrs1057516713
geneviewrs1057516713
scholarrs1057516713
googlers1057516713
pharmgkbrs1057516713
gwascentralrs1057516713
openSNPrs1057516713
23andMers1057516713
23andMe allrs1057516713
SNPshotrs1057516713
SNPdbers1057516713
MSV3drs1057516713
GWAS Ctlgrs1057516713
Max Magnitude0
ClinVar
Risk rs1057516713(G;G)
Alt rs1057516713(G;G)
Reference Rs1057516713(A;A)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98015302T>C
CLNSRC
CLNACC RCV000411699.1,