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rs6052761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6052761(C;C)
Make rs6052761(C;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position4676371
is asnp
is mentioned by
dbSNPrs6052761
ebirs6052761
HLIrs6052761
Exacrs6052761
Varsomers6052761
Maprs6052761
PheGenIrs6052761
hapmaprs6052761
1000 genomesrs6052761
hgdprs6052761
ensemblrs6052761
gopubmedrs6052761
geneviewrs6052761
scholarrs6052761
googlers6052761
pharmgkbrs6052761
gwascentralrs6052761
openSNPrs6052761
23andMers6052761
23andMe allrs6052761
SNP Nexus

SNPshotrs6052761
SNPdbers6052761
MSV3drs6052761
GWAS Ctlgrs6052761
GMAF0.1483
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs6052761
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary