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

rs1057517065

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517065(C;C)
Make rs1057517065(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position97691715
GeneDPYD
is asnp
is mentioned by
dbSNPrs1057517065
dbSNP (old)rs1057517065
ClinGenrs1057517065
ebirs1057517065
HLIrs1057517065
Exacrs1057517065
Gnomadrs1057517065
Varsomers1057517065
Maprs1057517065
PheGenIrs1057517065
Biobankrs1057517065
1000 genomesrs1057517065
hgdprs1057517065
ensemblrs1057517065
gopubmedrs1057517065
geneviewrs1057517065
scholarrs1057517065
googlers1057517065
pharmgkbrs1057517065
gwascentralrs1057517065
openSNPrs1057517065
23andMers1057517065
23andMe allrs1057517065
SNPshotrs1057517065
SNPdbers1057517065
MSV3drs1057517065
GWAS Ctlgrs1057517065
Max Magnitude0
ClinVar
Risk rs1057517065(C;C)
Alt rs1057517065(C;C)
Reference Rs1057517065(T;T)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 1
HGVS NC_000001.10:g.98157271A>G
CLNSRC
CLNACC RCV000409929.1,