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rs1057517055

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517055(-;-)
Make rs1057517055(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97373616
GeneDPYD, LOC105378867
is asnp
is mentioned by
dbSNPrs1057517055
dbSNP (classic)rs1057517055
ClinGenrs1057517055
ebirs1057517055
HLIrs1057517055
Exacrs1057517055
Gnomadrs1057517055
Varsomers1057517055
LitVarrs1057517055
Maprs1057517055
PheGenIrs1057517055
Biobankrs1057517055
1000 genomesrs1057517055
hgdprs1057517055
ensemblrs1057517055
geneviewrs1057517055
scholarrs1057517055
googlers1057517055
pharmgkbrs1057517055
gwascentralrs1057517055
openSNPrs1057517055
23andMers1057517055
23andMe allrs1057517055
SNPshotrs1057517055
SNPdbers1057517055
MSV3drs1057517055
GWAS Ctlgrs1057517055
Max Magnitude0
ClinVar
Risk rs1057517055(-;-)
Alt rs1057517055(-;-)
Reference Rs1057517055(A;A)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97839172delT
CLNSRC
CLNACC RCV000411454.1,