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rs6017787

From SNPedia

Orientationplus
Stabilizedplus
Make rs6017787(G;G)
Make rs6017787(G;T)
Make rs6017787(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position46346057
is asnp
is mentioned by
dbSNPrs6017787
ebirs6017787
HLIrs6017787
Exacrs6017787
Varsomers6017787
Maprs6017787
PheGenIrs6017787
hapmaprs6017787
1000 genomesrs6017787
hgdprs6017787
ensemblrs6017787
gopubmedrs6017787
geneviewrs6017787
scholarrs6017787
googlers6017787
pharmgkbrs6017787
gwascentralrs6017787
openSNPrs6017787
23andMers6017787
23andMe allrs6017787
SNP Nexus

SNPshotrs6017787
SNPdbers6017787
MSV3drs6017787
GWAS Ctlgrs6017787
GMAF0.3875
Max Magnitude
? (G;G) (G;T) (T;T) 28


GET Evidence
rs6017787
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.416667
summary