Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516388(A;A)
Make rs1057516388(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97450101
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516388
dbSNP (old)rs1057516388
ClinGenrs1057516388
ebirs1057516388
HLIrs1057516388
Exacrs1057516388
Gnomadrs1057516388
Varsomers1057516388
Maprs1057516388
PheGenIrs1057516388
Biobankrs1057516388
1000 genomesrs1057516388
hgdprs1057516388
ensemblrs1057516388
gopubmedrs1057516388
geneviewrs1057516388
scholarrs1057516388
googlers1057516388
pharmgkbrs1057516388
gwascentralrs1057516388
openSNPrs1057516388
23andMers1057516388
23andMe allrs1057516388
SNPshotrs1057516388
SNPdbers1057516388
MSV3drs1057516388
GWAS Ctlgrs1057516388
Max Magnitude0
ClinVar
Risk rs1057516388(A;A)
Alt rs1057516388(A;A)
Reference Rs1057516388(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97915657C>T
CLNSRC
CLNACC RCV000409426.1,