Have questions? Visit https://www.reddit.com/r/SNPedia

rs1801267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1801267(A;A)
Make rs1801267(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position97098598
GeneDPYD, DPYD-AS1
is asnp
is mentioned by
dbSNPrs1801267
ebirs1801267
HLIrs1801267
Exacrs1801267
Varsomers1801267
Maprs1801267
PheGenIrs1801267
hapmaprs1801267
1000 genomesrs1801267
hgdprs1801267
ensemblrs1801267
gopubmedrs1801267
geneviewrs1801267
scholarrs1801267
googlers1801267
pharmgkbrs1801267
gwascentralrs1801267
openSNPrs1801267
23andMers1801267
23andMe allrs1801267
SNP Nexus

SNPshotrs1801267
SNPdbers1801267
MSV3drs1801267
GWAS Ctlgrs1801267
Max Magnitude0
OMIM612779
Desc
Variant0006
Relatedalso


ClinVar
Risk rs1801267(A;A)
Alt rs1801267(A;A)
Reference rs1801267(G;G)
Significance Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD-AS1 DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97564154C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000466.2,