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rs659628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs659628(A;A)
Make rs659628(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position76889101
is asnp
is mentioned by
dbSNPrs659628
ebirs659628
HLIrs659628
Exacrs659628
Varsomers659628
Maprs659628
PheGenIrs659628
hapmaprs659628
1000 genomesrs659628
hgdprs659628
ensemblrs659628
gopubmedrs659628
geneviewrs659628
scholarrs659628
googlers659628
pharmgkbrs659628
gwascentralrs659628
openSNPrs659628
23andMers659628
23andMe allrs659628
SNP Nexus

SNPshotrs659628
SNPdbers659628
MSV3drs659628
GWAS Ctlgrs659628
GMAF0.08494
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs659628
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.09375
summary