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rs2052383

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2052383(G;G)
Make rs2052383(G;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position105547179
is asnp
is mentioned by
dbSNPrs2052383
ebirs2052383
HLIrs2052383
Exacrs2052383
Varsomers2052383
Maprs2052383
PheGenIrs2052383
hapmaprs2052383
1000 genomesrs2052383
hgdprs2052383
ensemblrs2052383
gopubmedrs2052383
geneviewrs2052383
scholarrs2052383
googlers2052383
pharmgkbrs2052383
gwascentralrs2052383
openSNPrs2052383
23andMers2052383
23andMe allrs2052383
SNP Nexus

SNPshotrs2052383
SNPdbers2052383
MSV3drs2052383
GWAS Ctlgrs2052383
GMAF0.3242
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GET Evidence
rs2052383
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.695312
summary