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rs888597

From SNPedia

Orientationplus
Stabilizedplus
Make rs888597(A;A)
Make rs888597(A;G)
Make rs888597(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position99992053
GeneCNTN5
is asnp
is mentioned by
dbSNPrs888597
ebirs888597
HLIrs888597
Exacrs888597
Varsomers888597
Maprs888597
PheGenIrs888597
hapmaprs888597
1000 genomesrs888597
hgdprs888597
ensemblrs888597
gopubmedrs888597
geneviewrs888597
scholarrs888597
googlers888597
pharmgkbrs888597
gwascentralrs888597
openSNPrs888597
23andMers888597
23andMe allrs888597
SNP Nexus

SNPshotrs888597
SNPdbers888597
MSV3drs888597
GWAS Ctlgrs888597
GMAF0.3343
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs888597
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.388889
summary