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rs8177517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs8177517(A;C)
Make rs8177517(C;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position160242388
GeneSLC22A2
is asnp
is mentioned by
dbSNPrs8177517
ebirs8177517
HLIrs8177517
Exacrs8177517
Varsomers8177517
Maprs8177517
PheGenIrs8177517
hapmaprs8177517
1000 genomesrs8177517
hgdprs8177517
ensemblrs8177517
gopubmedrs8177517
geneviewrs8177517
scholarrs8177517
googlers8177517
pharmgkbrs8177517
gwascentralrs8177517
openSNPrs8177517
23andMers8177517
23andMe allrs8177517
SNP Nexus

SNPshotrs8177517
SNPdbers8177517
MSV3drs8177517
GWAS Ctlgrs8177517
GMAF0.01102
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GET Evidence
SLC22A2-K432Q
aa_change Lys432Gln
aa_change_short K432Q
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.00817996
summary