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rs1065776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1065776(C;T)
Make rs1065776(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position152835839
GeneP2RY1
is asnp
is mentioned by
dbSNPrs1065776
ebirs1065776
HLIrs1065776
Exacrs1065776
Varsomers1065776
Maprs1065776
PheGenIrs1065776
hapmaprs1065776
1000 genomesrs1065776
hgdprs1065776
ensemblrs1065776
gopubmedrs1065776
geneviewrs1065776
scholarrs1065776
googlers1065776
pharmgkbrs1065776
gwascentralrs1065776
openSNPrs1065776
23andMers1065776
23andMe allrs1065776
SNP Nexus

SNPshotrs1065776
SNPdbers1065776
MSV3drs1065776
GWAS Ctlgrs1065776
GMAF0.08724
Max Magnitude0




GET Evidence
rs1065776
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0846812
summary