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rs9659092

From SNPedia

Orientationplus
Stabilizedplus
Make rs9659092(A;A)
Make rs9659092(A;G)
Make rs9659092(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position49977917
GeneAGBL4
is asnp
is mentioned by
dbSNPrs9659092
ebirs9659092
HLIrs9659092
Exacrs9659092
Varsomers9659092
Maprs9659092
PheGenIrs9659092
hapmaprs9659092
1000 genomesrs9659092
hgdprs9659092
ensemblrs9659092
gopubmedrs9659092
geneviewrs9659092
scholarrs9659092
googlers9659092
pharmgkbrs9659092
gwascentralrs9659092
openSNPrs9659092
23andMers9659092
23andMe allrs9659092
SNP Nexus

SNPshotrs9659092
SNPdbers9659092
MSV3drs9659092
GWAS Ctlgrs9659092
GMAF0.2952
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs9659092
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary