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rs1057516711

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516711(-;-)
Make rs1057516711(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97595107
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516711
dbSNP (old)rs1057516711
ClinGenrs1057516711
ebirs1057516711
HLIrs1057516711
Exacrs1057516711
Gnomadrs1057516711
Varsomers1057516711
LitVarrs1057516711
Maprs1057516711
PheGenIrs1057516711
Biobankrs1057516711
1000 genomesrs1057516711
hgdprs1057516711
ensemblrs1057516711
gopubmedrs1057516711
geneviewrs1057516711
scholarrs1057516711
googlers1057516711
pharmgkbrs1057516711
gwascentralrs1057516711
openSNPrs1057516711
23andMers1057516711
23andMe allrs1057516711
SNPshotrs1057516711
SNPdbers1057516711
MSV3drs1057516711
GWAS Ctlgrs1057516711
Max Magnitude0
ClinVar
Risk rs1057516711(-;-)
Alt rs1057516711(-;-)
Reference Rs1057516711(T;T)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98060663delA
CLNSRC
CLNACC RCV000411932.1,