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rs7915663

From SNPedia

Orientationplus
Stabilizedplus
Make rs7915663(A;A)
Make rs7915663(A;T)
Make rs7915663(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position86154279
GeneGRID1
is asnp
is mentioned by
dbSNPrs7915663
ebirs7915663
HLIrs7915663
Exacrs7915663
Varsomers7915663
Maprs7915663
PheGenIrs7915663
hapmaprs7915663
1000 genomesrs7915663
hgdprs7915663
ensemblrs7915663
gopubmedrs7915663
geneviewrs7915663
scholarrs7915663
googlers7915663
pharmgkbrs7915663
gwascentralrs7915663
openSNPrs7915663
23andMers7915663
23andMe allrs7915663
SNP Nexus

SNPshotrs7915663
SNPdbers7915663
MSV3drs7915663
GWAS Ctlgrs7915663
GMAF0.2094
Max Magnitude
? (A;A) (A;T) (T;T) 28


GET Evidence
rs7915663
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.289062
summary