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rs1057516696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516696(C;C)
Make rs1057516696(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97595167
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516696
dbSNP (old)rs1057516696
ClinGenrs1057516696
ebirs1057516696
HLIrs1057516696
Exacrs1057516696
Gnomadrs1057516696
Varsomers1057516696
Maprs1057516696
PheGenIrs1057516696
Biobankrs1057516696
1000 genomesrs1057516696
hgdprs1057516696
ensemblrs1057516696
gopubmedrs1057516696
geneviewrs1057516696
scholarrs1057516696
googlers1057516696
pharmgkbrs1057516696
gwascentralrs1057516696
openSNPrs1057516696
23andMers1057516696
23andMe allrs1057516696
SNPshotrs1057516696
SNPdbers1057516696
MSV3drs1057516696
GWAS Ctlgrs1057516696
Max Magnitude0
ClinVar
Risk rs1057516696(C;C)
Alt rs1057516696(C;C)
Reference Rs1057516696(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98060723C>G
CLNSRC
CLNACC RCV000409515.1,