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rs1057517126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517126(A;A)
Make rs1057517126(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97549559
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057517126
dbSNP (old)rs1057517126
ClinGenrs1057517126
ebirs1057517126
HLIrs1057517126
Exacrs1057517126
Gnomadrs1057517126
Varsomers1057517126
Maprs1057517126
PheGenIrs1057517126
Biobankrs1057517126
1000 genomesrs1057517126
hgdprs1057517126
ensemblrs1057517126
gopubmedrs1057517126
geneviewrs1057517126
scholarrs1057517126
googlers1057517126
pharmgkbrs1057517126
gwascentralrs1057517126
openSNPrs1057517126
23andMers1057517126
23andMe allrs1057517126
SNPshotrs1057517126
SNPdbers1057517126
MSV3drs1057517126
GWAS Ctlgrs1057517126
Max Magnitude0
ClinVar
Risk rs1057517126(A;A)
Alt rs1057517126(A;A)
Reference Rs1057517126(G;G)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98015115C>T
CLNSRC
CLNACC RCV000412072.1,