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rs1057516997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516997(-;-)
Make rs1057516997(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97699508
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516997
dbSNP (classic)rs1057516997
ClinGenrs1057516997
ebirs1057516997
HLIrs1057516997
Exacrs1057516997
Gnomadrs1057516997
Varsomers1057516997
LitVarrs1057516997
Maprs1057516997
PheGenIrs1057516997
Biobankrs1057516997
1000 genomesrs1057516997
hgdprs1057516997
ensemblrs1057516997
geneviewrs1057516997
scholarrs1057516997
googlers1057516997
pharmgkbrs1057516997
gwascentralrs1057516997
openSNPrs1057516997
23andMers1057516997
23andMe allrs1057516997
SNPshotrs1057516997
SNPdbers1057516997
MSV3drs1057516997
GWAS Ctlgrs1057516997
Max Magnitude0
ClinVar
Risk rs1057516997(-;-)
Alt rs1057516997(-;-)
Reference Rs1057516997(T;T)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98165064delA
CLNSRC
CLNACC RCV000410066.1,