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rs72547602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72547602(A;A)
Make rs72547602(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position97079133
GeneDPYD
is asnp
is mentioned by
dbSNPrs72547602
ebirs72547602
HLIrs72547602
Exacrs72547602
Varsomers72547602
Maprs72547602
PheGenIrs72547602
hapmaprs72547602
1000 genomesrs72547602
hgdprs72547602
ensemblrs72547602
gopubmedrs72547602
geneviewrs72547602
scholarrs72547602
googlers72547602
pharmgkbrs72547602
gwascentralrs72547602
openSNPrs72547602
23andMers72547602
23andMe allrs72547602
SNP Nexus

SNPshotrs72547602
SNPdbers72547602
MSV3drs72547602
GWAS Ctlgrs72547602
Max Magnitude0
OMIM612779
Desc
Variant0002
Relatedalso
ClinVar
Risk rs72547602(A;A)
Alt rs72547602(A;A)
Reference rs72547602(T;T)
Significance Pathogenic
Disease Fluorouracil response
Variation info
Gene DPYD
CLNDBN Fluorouracil response
Reversed 0
HGVS NC_000001.10:g.97544689T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030869.2,