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rs1057516761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516761(-;-)
Make rs1057516761(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97573783
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516761
dbSNP (old)rs1057516761
ClinGenrs1057516761
ebirs1057516761
HLIrs1057516761
Exacrs1057516761
Gnomadrs1057516761
Varsomers1057516761
LitVarrs1057516761
Maprs1057516761
PheGenIrs1057516761
Biobankrs1057516761
1000 genomesrs1057516761
hgdprs1057516761
ensemblrs1057516761
gopubmedrs1057516761
geneviewrs1057516761
scholarrs1057516761
googlers1057516761
pharmgkbrs1057516761
gwascentralrs1057516761
openSNPrs1057516761
23andMers1057516761
23andMe allrs1057516761
SNPshotrs1057516761
SNPdbers1057516761
MSV3drs1057516761
GWAS Ctlgrs1057516761
Max Magnitude0
ClinVar
Risk rs1057516761(-;-)
Alt rs1057516761(-;-)
Reference Rs1057516761(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98039339delC
CLNSRC
CLNACC RCV000411796.1,