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

rs1057516671

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516671(G;T)
Make rs1057516671(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97450133
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516671
dbSNP (old)rs1057516671
ClinGenrs1057516671
ebirs1057516671
HLIrs1057516671
Exacrs1057516671
Gnomadrs1057516671
Varsomers1057516671
Maprs1057516671
PheGenIrs1057516671
Biobankrs1057516671
1000 genomesrs1057516671
hgdprs1057516671
ensemblrs1057516671
gopubmedrs1057516671
geneviewrs1057516671
scholarrs1057516671
googlers1057516671
pharmgkbrs1057516671
gwascentralrs1057516671
openSNPrs1057516671
23andMers1057516671
23andMe allrs1057516671
SNPshotrs1057516671
SNPdbers1057516671
MSV3drs1057516671
GWAS Ctlgrs1057516671
Max Magnitude0
ClinVar
Risk rs1057516671(T;T)
Alt rs1057516671(T;T)
Reference Rs1057516671(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97915689C>A
CLNSRC
CLNACC RCV000410030.1,