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rs486060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs486060(C;C)
Make rs486060(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position53591884
is asnp
is mentioned by
dbSNPrs486060
ebirs486060
HLIrs486060
Exacrs486060
Varsomers486060
Maprs486060
PheGenIrs486060
hapmaprs486060
1000 genomesrs486060
hgdprs486060
ensemblrs486060
gopubmedrs486060
geneviewrs486060
scholarrs486060
googlers486060
pharmgkbrs486060
gwascentralrs486060
openSNPrs486060
23andMers486060
23andMe allrs486060
SNP Nexus

SNPshotrs486060
SNPdbers486060
MSV3drs486060
GWAS Ctlgrs486060
GMAF0.1304
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs486060
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.164062
summary