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rs1801266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common genotype
Make rs1801266(C;T)
Make rs1801266(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position97691776
GeneDPYD
is asnp
is mentioned by
dbSNPrs1801266
dbSNP (classic)rs1801266
ClinGenrs1801266
ebirs1801266
HLIrs1801266
Exacrs1801266
Gnomadrs1801266
Varsomers1801266
LitVarrs1801266
Maprs1801266
PheGenIrs1801266
Biobankrs1801266
1000 genomesrs1801266
hgdprs1801266
ensemblrs1801266
geneviewrs1801266
scholarrs1801266
googlers1801266
pharmgkbrs1801266
gwascentralrs1801266
openSNPrs1801266
23andMers1801266
SNPshotrs1801266
SNPdbers1801266
MSV3drs1801266
GWAS Ctlgrs1801266
Max Magnitude0


ClinVar
Risk rs1801266(T;T)
Alt rs1801266(T;T)
Reference Rs1801266(C;C)
Significance Unknown
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98157332G>A
CLNSRC
CLNACC RCV000362597.1,