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rs1059231

From SNPedia

Orientationminus
Stabilizedminus
Make rs1059231(C;C)
Make rs1059231(C;T)
Make rs1059231(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33320494
GeneDAXX
is asnp
is mentioned by
dbSNPrs1059231
ebirs1059231
HLIrs1059231
Exacrs1059231
Varsomers1059231
Maprs1059231
PheGenIrs1059231
hapmaprs1059231
1000 genomesrs1059231
hgdprs1059231
ensemblrs1059231
gopubmedrs1059231
geneviewrs1059231
scholarrs1059231
googlers1059231
pharmgkbrs1059231
gwascentralrs1059231
openSNPrs1059231
23andMers1059231
23andMe allrs1059231
SNP Nexus

SNPshotrs1059231
SNPdbers1059231
MSV3drs1059231
GWAS Ctlgrs1059231
GMAF0.2401
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs1059231
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.218721
summary