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

rs1057516405

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057516405(A;A)
Make rs1057516405(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97883262
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516405
dbSNP (old)rs1057516405
ClinGenrs1057516405
ebirs1057516405
HLIrs1057516405
Exacrs1057516405
Gnomadrs1057516405
Varsomers1057516405
Maprs1057516405
PheGenIrs1057516405
Biobankrs1057516405
1000 genomesrs1057516405
hgdprs1057516405
ensemblrs1057516405
gopubmedrs1057516405
geneviewrs1057516405
scholarrs1057516405
googlers1057516405
pharmgkbrs1057516405
gwascentralrs1057516405
openSNPrs1057516405
23andMers1057516405
23andMe allrs1057516405
SNPshotrs1057516405
SNPdbers1057516405
MSV3drs1057516405
GWAS Ctlgrs1057516405
Max Magnitude0
ClinVar
Risk rs1057516405(A;A)
Alt rs1057516405(A;A)
Reference Rs1057516405(T;T)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98348818A>T
CLNSRC
CLNACC RCV000410919.1,