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rs1057517189

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517189(-;-)
Make rs1057517189(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97573788
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057517189
dbSNP (old)rs1057517189
ClinGenrs1057517189
ebirs1057517189
HLIrs1057517189
Exacrs1057517189
Gnomadrs1057517189
Varsomers1057517189
Maprs1057517189
PheGenIrs1057517189
Biobankrs1057517189
1000 genomesrs1057517189
hgdprs1057517189
ensemblrs1057517189
gopubmedrs1057517189
geneviewrs1057517189
scholarrs1057517189
googlers1057517189
pharmgkbrs1057517189
gwascentralrs1057517189
openSNPrs1057517189
23andMers1057517189
23andMe allrs1057517189
SNPshotrs1057517189
SNPdbers1057517189
MSV3drs1057517189
GWAS Ctlgrs1057517189
Max Magnitude0
ClinVar
Risk rs1057517189(-;-)
Alt rs1057517189(-;-)
Reference Rs1057517189(C;C)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98039344delG
CLNSRC
CLNACC RCV000410794.1,