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rs1057516615

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516615(-;-)
Make rs1057516615(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97549566
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516615
dbSNP (old)rs1057516615
ClinGenrs1057516615
ebirs1057516615
HLIrs1057516615
Exacrs1057516615
Gnomadrs1057516615
Varsomers1057516615
Maprs1057516615
PheGenIrs1057516615
Biobankrs1057516615
1000 genomesrs1057516615
hgdprs1057516615
ensemblrs1057516615
gopubmedrs1057516615
geneviewrs1057516615
scholarrs1057516615
googlers1057516615
pharmgkbrs1057516615
gwascentralrs1057516615
openSNPrs1057516615
23andMers1057516615
23andMe allrs1057516615
SNPshotrs1057516615
SNPdbers1057516615
MSV3drs1057516615
GWAS Ctlgrs1057516615
Max Magnitude0
ClinVar
Risk rs1057516615(-;-)
Alt rs1057516615(-;-)
Reference Rs1057516615(C;C)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98015122delG
CLNSRC
CLNACC RCV000409377.1,