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rs7537752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7537752(C;G)
Make rs7537752(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position109931820
is asnp
is mentioned by
dbSNPrs7537752
ebirs7537752
HLIrs7537752
Exacrs7537752
Varsomers7537752
Maprs7537752
PheGenIrs7537752
hapmaprs7537752
1000 genomesrs7537752
hgdprs7537752
ensemblrs7537752
gopubmedrs7537752
geneviewrs7537752
scholarrs7537752
googlers7537752
pharmgkbrs7537752
gwascentralrs7537752
openSNPrs7537752
23andMers7537752
23andMe allrs7537752
SNP Nexus

SNPshotrs7537752
SNPdbers7537752
MSV3drs7537752
GWAS Ctlgrs7537752
GMAF0.4357
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs7537752
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.476562
summary