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rs959091

From SNPedia

Orientationplus
Stabilizedplus
Make rs959091(A;A)
Make rs959091(A;G)
Make rs959091(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position23775451
GeneELAVL2
is asnp
is mentioned by
dbSNPrs959091
ebirs959091
HLIrs959091
Exacrs959091
Varsomers959091
Maprs959091
PheGenIrs959091
hapmaprs959091
1000 genomesrs959091
hgdprs959091
ensemblrs959091
gopubmedrs959091
geneviewrs959091
scholarrs959091
googlers959091
pharmgkbrs959091
gwascentralrs959091
openSNPrs959091
23andMers959091
23andMe allrs959091
SNP Nexus

SNPshotrs959091
SNPdbers959091
MSV3drs959091
GWAS Ctlgrs959091
GMAF0.1768
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs959091
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary