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rs9662927

From SNPedia

Orientationplus
Stabilizedplus
Make rs9662927(A;A)
Make rs9662927(A;G)
Make rs9662927(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position240375652
GeneFMN2
is asnp
is mentioned by
dbSNPrs9662927
ebirs9662927
HLIrs9662927
Exacrs9662927
Varsomers9662927
Maprs9662927
PheGenIrs9662927
hapmaprs9662927
1000 genomesrs9662927
hgdprs9662927
ensemblrs9662927
gopubmedrs9662927
geneviewrs9662927
scholarrs9662927
googlers9662927
pharmgkbrs9662927
gwascentralrs9662927
openSNPrs9662927
23andMers9662927
23andMe allrs9662927
SNP Nexus

SNPshotrs9662927
SNPdbers9662927
MSV3drs9662927
GWAS Ctlgrs9662927
GMAF0.4068
Max Magnitude
? (A;A) (A;G) (G;G) 28



GET Evidence
rs9662927
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.640625
summary