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rs186364861

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs186364861(A;A)
Make rs186364861(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position48037798
GeneNUDT15
is asnp
is mentioned by
dbSNPrs186364861
ebirs186364861
HLIrs186364861
Exacrs186364861
Varsomers186364861
Maprs186364861
PheGenIrs186364861
hapmaprs186364861
1000 genomesrs186364861
hgdprs186364861
ensemblrs186364861
gopubmedrs186364861
geneviewrs186364861
scholarrs186364861
googlers186364861
pharmgkbrs186364861
gwascentralrs186364861
openSNPrs186364861
23andMers186364861
23andMe allrs186364861
SNP Nexus

SNPshotrs186364861
SNPdbers186364861
MSV3drs186364861
GWAS Ctlgrs186364861
Max Magnitude0
ClinVar
Risk rs186364861(A;A)
Alt rs186364861(A;A)
Reference rs186364861(G;G)
Significance Drug-response
Disease Thiopurines
Variation info
Gene NUDT15 SUCLA2
CLNDBN Thiopurines, poor metabolism of, 2
Reversed 0
HGVS NC_000013.10:g.48611934G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210850.1,