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rs497710

From SNPedia

Orientationplus
Stabilizedplus
Make rs497710(A;A)
Make rs497710(A;G)
Make rs497710(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position66799248
GeneINSL5
is asnp
is mentioned by
dbSNPrs497710
ebirs497710
HLIrs497710
Exacrs497710
Varsomers497710
Maprs497710
PheGenIrs497710
hapmaprs497710
1000 genomesrs497710
hgdprs497710
ensemblrs497710
gopubmedrs497710
geneviewrs497710
scholarrs497710
googlers497710
pharmgkbrs497710
gwascentralrs497710
openSNPrs497710
23andMers497710
23andMe allrs497710
SNP Nexus

SNPshotrs497710
SNPdbers497710
MSV3drs497710
GWAS Ctlgrs497710
GMAF0.1175
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs497710
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.84375
summary