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rs1057517018

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517018(-;-)
Make rs1057517018(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97515795
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057517018
dbSNP (old)rs1057517018
ClinGenrs1057517018
ebirs1057517018
HLIrs1057517018
Exacrs1057517018
Gnomadrs1057517018
Varsomers1057517018
Maprs1057517018
PheGenIrs1057517018
Biobankrs1057517018
1000 genomesrs1057517018
hgdprs1057517018
ensemblrs1057517018
gopubmedrs1057517018
geneviewrs1057517018
scholarrs1057517018
googlers1057517018
pharmgkbrs1057517018
gwascentralrs1057517018
openSNPrs1057517018
23andMers1057517018
23andMe allrs1057517018
SNPshotrs1057517018
SNPdbers1057517018
MSV3drs1057517018
GWAS Ctlgrs1057517018
Max Magnitude0
ClinVar
Risk rs1057517018(-;-)
Alt rs1057517018(-;-)
Reference Rs1057517018(A;A)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97981351delT
CLNSRC
CLNACC RCV000412205.1,