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rs6566561

From SNPedia

Orientationplus
Stabilizedplus
Make rs6566561(A;A)
Make rs6566561(A;G)
Make rs6566561(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position71686954
is asnp
is mentioned by
dbSNPrs6566561
ebirs6566561
HLIrs6566561
Exacrs6566561
Varsomers6566561
Maprs6566561
PheGenIrs6566561
hapmaprs6566561
1000 genomesrs6566561
hgdprs6566561
ensemblrs6566561
gopubmedrs6566561
geneviewrs6566561
scholarrs6566561
googlers6566561
pharmgkbrs6566561
gwascentralrs6566561
openSNPrs6566561
23andMers6566561
23andMe allrs6566561
SNP Nexus

SNPshotrs6566561
SNPdbers6566561
MSV3drs6566561
GWAS Ctlgrs6566561
GMAF0.2888
Max Magnitude
? (A;A) (A;G) (G;G) 28



GET Evidence
rs6566561
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.273438
summary