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rs1057516710

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516710(-;-)
Make rs1057516710(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97382397
GeneDPYD, LOC105378867
is asnp
is mentioned by
dbSNPrs1057516710
dbSNP (old)rs1057516710
ClinGenrs1057516710
ebirs1057516710
HLIrs1057516710
Exacrs1057516710
Gnomadrs1057516710
Varsomers1057516710
Maprs1057516710
PheGenIrs1057516710
Biobankrs1057516710
1000 genomesrs1057516710
hgdprs1057516710
ensemblrs1057516710
gopubmedrs1057516710
geneviewrs1057516710
scholarrs1057516710
googlers1057516710
pharmgkbrs1057516710
gwascentralrs1057516710
openSNPrs1057516710
23andMers1057516710
23andMe allrs1057516710
SNPshotrs1057516710
SNPdbers1057516710
MSV3drs1057516710
GWAS Ctlgrs1057516710
Max Magnitude0
ClinVar
Risk rs1057516710(-;-)
Alt rs1057516710(-;-)
Reference Rs1057516710(C;C)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97847953delG
CLNSRC
CLNACC RCV000410448.1,