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rs7125266

From SNPedia

Orientationplus
Stabilizedplus
Make rs7125266(A;A)
Make rs7125266(A;G)
Make rs7125266(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position99995020
GeneCNTN5
is asnp
is mentioned by
dbSNPrs7125266
ebirs7125266
HLIrs7125266
Exacrs7125266
Varsomers7125266
Maprs7125266
PheGenIrs7125266
hapmaprs7125266
1000 genomesrs7125266
hgdprs7125266
ensemblrs7125266
gopubmedrs7125266
geneviewrs7125266
scholarrs7125266
googlers7125266
pharmgkbrs7125266
gwascentralrs7125266
openSNPrs7125266
23andMers7125266
23andMe allrs7125266
SNP Nexus

SNPshotrs7125266
SNPdbers7125266
MSV3drs7125266
GWAS Ctlgrs7125266
GMAF0.3655
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs7125266
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.416667
summary