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rs1057516968

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516968(C;T)
Make rs1057516968(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97515785
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516968
dbSNP (classic)rs1057516968
ClinGenrs1057516968
ebirs1057516968
HLIrs1057516968
Exacrs1057516968
Gnomadrs1057516968
Varsomers1057516968
LitVarrs1057516968
Maprs1057516968
PheGenIrs1057516968
Biobankrs1057516968
1000 genomesrs1057516968
hgdprs1057516968
ensemblrs1057516968
geneviewrs1057516968
scholarrs1057516968
googlers1057516968
pharmgkbrs1057516968
gwascentralrs1057516968
openSNPrs1057516968
23andMers1057516968
23andMe allrs1057516968
SNPshotrs1057516968
SNPdbers1057516968
MSV3drs1057516968
GWAS Ctlgrs1057516968
Max Magnitude0
ClinVar
Risk rs1057516968(T;T)
Alt rs1057516968(T;T)
Reference Rs1057516968(C;C)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97981341G>A
CLNSRC
CLNACC RCV000409394.1,