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rs7913723

From SNPedia

Orientationplus
Stabilizedplus
Make rs7913723(C;C)
Make rs7913723(C;G)
Make rs7913723(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position6309187
GeneGSX2
is asnp
is mentioned by
dbSNPrs7913723
ebirs7913723
HLIrs7913723
Exacrs7913723
Varsomers7913723
Maprs7913723
PheGenIrs7913723
hapmaprs7913723
1000 genomesrs7913723
hgdprs7913723
ensemblrs7913723
gopubmedrs7913723
geneviewrs7913723
scholarrs7913723
googlers7913723
pharmgkbrs7913723
gwascentralrs7913723
openSNPrs7913723
23andMers7913723
23andMe allrs7913723
SNP Nexus

SNPshotrs7913723
SNPdbers7913723
MSV3drs7913723
GWAS Ctlgrs7913723
GMAF0.1047
Max Magnitude
? (C;C) (C;G) (G;G) 28


GET Evidence
rs7913723
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.132812
summary