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rs2184711

From SNPedia

Orientationminus
Stabilizedminus
Make rs2184711(C;C)
Make rs2184711(C;T)
Make rs2184711(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position240391688
GeneFMN2
is asnp
is mentioned by
dbSNPrs2184711
ebirs2184711
HLIrs2184711
Exacrs2184711
Varsomers2184711
Maprs2184711
PheGenIrs2184711
hapmaprs2184711
1000 genomesrs2184711
hgdprs2184711
ensemblrs2184711
gopubmedrs2184711
geneviewrs2184711
scholarrs2184711
googlers2184711
pharmgkbrs2184711
gwascentralrs2184711
openSNPrs2184711
23andMers2184711
23andMe allrs2184711
SNP Nexus

SNPshotrs2184711
SNPdbers2184711
MSV3drs2184711
GWAS Ctlgrs2184711
GMAF0.4151
Max Magnitude
? (C;C) (C;T) (T;T) 28



GET Evidence
rs2184711
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.632812
summary