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rs6539870

From SNPedia

Orientationplus
Stabilizedplus
Make rs6539870(A;A)
Make rs6539870(A;G)
Make rs6539870(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position84849902
is asnp
is mentioned by
dbSNPrs6539870
ebirs6539870
HLIrs6539870
Exacrs6539870
Varsomers6539870
Maprs6539870
PheGenIrs6539870
hapmaprs6539870
1000 genomesrs6539870
hgdprs6539870
ensemblrs6539870
gopubmedrs6539870
geneviewrs6539870
scholarrs6539870
googlers6539870
pharmgkbrs6539870
gwascentralrs6539870
openSNPrs6539870
23andMers6539870
23andMe allrs6539870
SNP Nexus

SNPshotrs6539870
SNPdbers6539870
MSV3drs6539870
GWAS Ctlgrs6539870
GMAF0.2773
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs6539870
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.375
summary