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rs267606774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606774(G;T)
Make rs267606774(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position104424247
GeneDPYS
is asnp
is mentioned by
dbSNPrs267606774
ebirs267606774
HLIrs267606774
Exacrs267606774
Varsomers267606774
Maprs267606774
PheGenIrs267606774
hapmaprs267606774
1000 genomesrs267606774
hgdprs267606774
ensemblrs267606774
gopubmedrs267606774
geneviewrs267606774
scholarrs267606774
googlers267606774
pharmgkbrs267606774
gwascentralrs267606774
openSNPrs267606774
23andMers267606774
23andMe allrs267606774
SNP Nexus

SNPshotrs267606774
SNPdbers267606774
MSV3drs267606774
GWAS Ctlgrs267606774
Max Magnitude0
ClinVar
Risk rs267606774(T;T)
Alt rs267606774(T;T)
Reference rs267606774(G;G)
Significance Pathogenic
Disease Dihydropyrimidinase deficiency
Variation info
Gene DPYS
CLNDBN Dihydropyrimidinase deficiency
Reversed 1
HGVS NC_000008.10:g.105436475C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000210.4,