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rs7664751

From SNPedia

Orientationplus
Stabilizedplus
Make rs7664751(A;A)
Make rs7664751(A;G)
Make rs7664751(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position33728311
is asnp
is mentioned by
dbSNPrs7664751
ebirs7664751
HLIrs7664751
Exacrs7664751
Varsomers7664751
Maprs7664751
PheGenIrs7664751
hapmaprs7664751
1000 genomesrs7664751
hgdprs7664751
ensemblrs7664751
gopubmedrs7664751
geneviewrs7664751
scholarrs7664751
googlers7664751
pharmgkbrs7664751
gwascentralrs7664751
openSNPrs7664751
23andMers7664751
23andMe allrs7664751
SNP Nexus

SNPshotrs7664751
SNPdbers7664751
MSV3drs7664751
GWAS Ctlgrs7664751
GMAF0.2658
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7664751
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.261905
summary