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rs460869

From SNPedia

Orientationplus
Stabilizedplus
Make rs460869(A;A)
Make rs460869(A;G)
Make rs460869(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position46449335
is asnp
is mentioned by
dbSNPrs460869
ebirs460869
HLIrs460869
Exacrs460869
Varsomers460869
Maprs460869
PheGenIrs460869
hapmaprs460869
1000 genomesrs460869
hgdprs460869
ensemblrs460869
gopubmedrs460869
geneviewrs460869
scholarrs460869
googlers460869
pharmgkbrs460869
gwascentralrs460869
openSNPrs460869
23andMers460869
23andMe allrs460869
SNP Nexus

SNPshotrs460869
SNPdbers460869
MSV3drs460869
GWAS Ctlgrs460869
GMAF0.393
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs460869
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.507812
summary