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rs701265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs701265(A;G)
Make rs701265(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position152836568
GeneP2RY1
is asnp
is mentioned by
dbSNPrs701265
ebirs701265
HLIrs701265
Exacrs701265
Varsomers701265
Maprs701265
PheGenIrs701265
hapmaprs701265
1000 genomesrs701265
hgdprs701265
ensemblrs701265
gopubmedrs701265
geneviewrs701265
scholarrs701265
googlers701265
pharmgkbrs701265
gwascentralrs701265
openSNPrs701265
23andMers701265
23andMe allrs701265
SNP Nexus

SNPshotrs701265
SNPdbers701265
MSV3drs701265
GWAS Ctlgrs701265
GMAF0.3375
Max Magnitude0
? (A;A) (A;G) (G;G) 28



GET Evidence
rs701265
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.331195
summary



[PMID 22574824OA-icon.png] P2RY1 and P2RY12 polymorphisms and on-aspirin platelet reactivity in patients with coronary artery disease


[PMID 23828624] Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome.