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rs59086055

From SNPedia

Orientationplus
Stabilizedplus
Make rs59086055(A;A)
Make rs59086055(A;G)
Make rs59086055(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position97450190
GeneDPYD
is asnp
is mentioned by
dbSNPrs59086055
dbSNP (old)rs59086055
ClinGenrs59086055
ebirs59086055
HLIrs59086055
Exacrs59086055
Varsomers59086055
Maprs59086055
PheGenIrs59086055
Biobankrs59086055
1000 genomesrs59086055
hgdprs59086055
ensemblrs59086055
gopubmedrs59086055
geneviewrs59086055
scholarrs59086055
googlers59086055
pharmgkbrs59086055
gwascentralrs59086055
openSNPrs59086055
23andMers59086055
23andMe allrs59086055
SNP Nexus

SNPshotrs59086055
SNPdbers59086055
MSV3drs59086055
GWAS Ctlgrs59086055
Max Magnitude


ClinVar
Risk rs59086055(A;A)
Alt rs59086055(A;A)
Reference rs59086055(G;G)
Significance Unknown
Disease not specified
Variation info
Gene DPYD
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.97915746G>A
CLNSRC
CLNACC RCV000280781.1,