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rs1057516356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516356(C;C)
Make rs1057516356(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97721672
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057516356
dbSNP (old)rs1057516356
ClinGenrs1057516356
ebirs1057516356
HLIrs1057516356
Exacrs1057516356
Gnomadrs1057516356
Varsomers1057516356
Maprs1057516356
PheGenIrs1057516356
Biobankrs1057516356
1000 genomesrs1057516356
hgdprs1057516356
ensemblrs1057516356
gopubmedrs1057516356
geneviewrs1057516356
scholarrs1057516356
googlers1057516356
pharmgkbrs1057516356
gwascentralrs1057516356
openSNPrs1057516356
23andMers1057516356
23andMe allrs1057516356
SNPshotrs1057516356
SNPdbers1057516356
MSV3drs1057516356
GWAS Ctlgrs1057516356
Max Magnitude0
ClinVar
Risk rs1057516356(C;C)
Alt rs1057516356(C;C)
Reference Rs1057516356(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98187228C>G
CLNSRC
CLNACC RCV000409647.1,