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rs1057516357

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516357(G;T)
Make rs1057516357(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97573759
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516357
dbSNP (old)rs1057516357
ClinGenrs1057516357
ebirs1057516357
HLIrs1057516357
Exacrs1057516357
Gnomadrs1057516357
Varsomers1057516357
Maprs1057516357
PheGenIrs1057516357
Biobankrs1057516357
1000 genomesrs1057516357
hgdprs1057516357
ensemblrs1057516357
gopubmedrs1057516357
geneviewrs1057516357
scholarrs1057516357
googlers1057516357
pharmgkbrs1057516357
gwascentralrs1057516357
openSNPrs1057516357
23andMers1057516357
23andMe allrs1057516357
SNPshotrs1057516357
SNPdbers1057516357
MSV3drs1057516357
GWAS Ctlgrs1057516357
Max Magnitude0
ClinVar
Risk rs1057516357(T;T)
Alt rs1057516357(T;T)
Reference Rs1057516357(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98039315C>A
CLNSRC
CLNACC RCV000412433.1,