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rs9826507

From SNPedia

Orientationplus
Stabilizedplus
Make rs9826507(A;A)
Make rs9826507(A;G)
Make rs9826507(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position137072544
is asnp
is mentioned by
dbSNPrs9826507
ebirs9826507
HLIrs9826507
Exacrs9826507
Varsomers9826507
Maprs9826507
PheGenIrs9826507
hapmaprs9826507
1000 genomesrs9826507
hgdprs9826507
ensemblrs9826507
gopubmedrs9826507
geneviewrs9826507
scholarrs9826507
googlers9826507
pharmgkbrs9826507
gwascentralrs9826507
openSNPrs9826507
23andMers9826507
23andMe allrs9826507
SNP Nexus

SNPshotrs9826507
SNPdbers9826507
MSV3drs9826507
GWAS Ctlgrs9826507
GMAF0.3049
Max Magnitude


GET Evidence
rs9826507
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.4
summary