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rs9662388

From SNPedia

Orientationplus
Stabilizedplus
Make rs9662388(A;A)
Make rs9662388(A;G)
Make rs9662388(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position240388923
GeneFMN2
is asnp
is mentioned by
dbSNPrs9662388
ebirs9662388
HLIrs9662388
Exacrs9662388
Varsomers9662388
Maprs9662388
PheGenIrs9662388
hapmaprs9662388
1000 genomesrs9662388
hgdprs9662388
ensemblrs9662388
gopubmedrs9662388
geneviewrs9662388
scholarrs9662388
googlers9662388
pharmgkbrs9662388
gwascentralrs9662388
openSNPrs9662388
23andMers9662388
23andMe allrs9662388
SNP Nexus

SNPshotrs9662388
SNPdbers9662388
MSV3drs9662388
GWAS Ctlgrs9662388
GMAF0.1538
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs9662388
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.15625
summary