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rs9789480

From SNPedia

Orientationplus
Stabilizedplus
Make rs9789480(A;A)
Make rs9789480(A;C)
Make rs9789480(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position198182902
is asnp
is mentioned by
dbSNPrs9789480
ebirs9789480
HLIrs9789480
Exacrs9789480
Varsomers9789480
Maprs9789480
PheGenIrs9789480
hapmaprs9789480
1000 genomesrs9789480
hgdprs9789480
ensemblrs9789480
gopubmedrs9789480
geneviewrs9789480
scholarrs9789480
googlers9789480
pharmgkbrs9789480
gwascentralrs9789480
openSNPrs9789480
23andMers9789480
23andMe allrs9789480
SNP Nexus

SNPshotrs9789480
SNPdbers9789480
MSV3drs9789480
GWAS Ctlgrs9789480
GMAF0.3246
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs9789480
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary