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rs1057517396

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517396(-;T)
Make rs1057517396(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97373579
GeneDPYD, LOC105378867
is asnp
is mentioned by
dbSNPrs1057517396
dbSNP (old)rs1057517396
ClinGenrs1057517396
ebirs1057517396
HLIrs1057517396
Exacrs1057517396
Gnomadrs1057517396
Varsomers1057517396
LitVarrs1057517396
Maprs1057517396
PheGenIrs1057517396
Biobankrs1057517396
1000 genomesrs1057517396
hgdprs1057517396
ensemblrs1057517396
gopubmedrs1057517396
geneviewrs1057517396
scholarrs1057517396
googlers1057517396
pharmgkbrs1057517396
gwascentralrs1057517396
openSNPrs1057517396
23andMers1057517396
23andMe allrs1057517396
SNPshotrs1057517396
SNPdbers1057517396
MSV3drs1057517396
GWAS Ctlgrs1057517396
Max Magnitude0
ClinVar
Risk rs1057517396(T;T)
Alt rs1057517396(T;T)
Reference Rs1057517396(-;-)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.97839136dupA
CLNSRC
CLNACC RCV000411299.1,