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rs773499329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGCCCACAGGCCAGG;CTGCCCACAGGCCAGG) 0 common in clinvar
Make rs773499329(-;-)
Make rs773499329(-;CTGCCCACAGGCCAGG)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position97373561
GeneDPYD, LOC105378867
is asnp
is mentioned by
dbSNPrs773499329
dbSNP (old)rs773499329
ClinGenrs773499329
ebirs773499329
HLIrs773499329
Exacrs773499329
Varsomers773499329
Maprs773499329
PheGenIrs773499329
Biobankrs773499329
1000 genomesrs773499329
hgdprs773499329
ensemblrs773499329
gopubmedrs773499329
geneviewrs773499329
scholarrs773499329
googlers773499329
pharmgkbrs773499329
gwascentralrs773499329
openSNPrs773499329
23andMers773499329
23andMe allrs773499329
SNP Nexus

SNPshotrs773499329
SNPdbers773499329
MSV3drs773499329
GWAS Ctlgrs773499329
Max Magnitude0
ClinVar
Risk rs773499329(-;-)
Alt rs773499329(-;-)
Reference Rs773499329(CTGCCCACAGGCCAGG;CTGCCCACAGGCCAGG)
Significance Probable-Pathogenic
Disease Dihydropyrimidine dehydrogenase deficiency
Variation info
Gene DPYD
CLNDBN Dihydropyrimidine dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.97839117_97839132del16
CLNSRC
CLNACC RCV000169225.1,