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rs7086128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7086128(A;G)
Make rs7086128(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position124898804
is asnp
is mentioned by
dbSNPrs7086128
ebirs7086128
HLIrs7086128
Exacrs7086128
Varsomers7086128
Maprs7086128
PheGenIrs7086128
hapmaprs7086128
1000 genomesrs7086128
hgdprs7086128
ensemblrs7086128
gopubmedrs7086128
geneviewrs7086128
scholarrs7086128
googlers7086128
pharmgkbrs7086128
gwascentralrs7086128
openSNPrs7086128
23andMers7086128
23andMe allrs7086128
SNP Nexus

SNPshotrs7086128
SNPdbers7086128
MSV3drs7086128
GWAS Ctlgrs7086128
GMAF0.1777
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7086128
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.166667
summary