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rs74423290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74423290(C;G)
Make rs74423290(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position18133884
GeneTPMT
is asnp
is mentioned by
dbSNPrs74423290
ebirs74423290
HLIrs74423290
Exacrs74423290
Varsomers74423290
Maprs74423290
PheGenIrs74423290
hapmaprs74423290
1000 genomesrs74423290
hgdprs74423290
ensemblrs74423290
gopubmedrs74423290
geneviewrs74423290
scholarrs74423290
googlers74423290
pharmgkbrs74423290
gwascentralrs74423290
openSNPrs74423290
23andMers74423290
23andMe allrs74423290
SNP Nexus

SNPshotrs74423290
SNPdbers74423290
MSV3drs74423290
GWAS Ctlgrs74423290
Max Magnitude0
OMIM187680
Desc
Variant0007
Relatedalso
ClinVar
Risk rs74423290(G;G)
Alt rs74423290(G;G)
Reference rs74423290(C;C)
Significance Drug-response
Disease Thiopurine methyltransferase deficiency
Variation info
Gene TPMT
CLNDBN Thiopurine methyltransferase deficiency
Reversed 1
HGVS NC_000006.11:g.18134115G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013564.25,