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rs9661599

From SNPedia

Orientationplus
Stabilizedplus
Make rs9661599(A;A)
Make rs9661599(A;T)
Make rs9661599(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position240384769
GeneFMN2
is asnp
is mentioned by
dbSNPrs9661599
ebirs9661599
HLIrs9661599
Exacrs9661599
Varsomers9661599
Maprs9661599
PheGenIrs9661599
hapmaprs9661599
1000 genomesrs9661599
hgdprs9661599
ensemblrs9661599
gopubmedrs9661599
geneviewrs9661599
scholarrs9661599
googlers9661599
pharmgkbrs9661599
gwascentralrs9661599
openSNPrs9661599
23andMers9661599
23andMe allrs9661599
SNP Nexus

SNPshotrs9661599
SNPdbers9661599
MSV3drs9661599
GWAS Ctlgrs9661599
GMAF0.416
Max Magnitude
? (A;A) (A;T) (T;T) 28


GET Evidence
rs9661599
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.625
summary