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rs10802866

From SNPedia

Orientationplus
Stabilizedplus
Make rs10802866(C;C)
Make rs10802866(C;T)
Make rs10802866(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position240377711
GeneFMN2
is asnp
is mentioned by
dbSNPrs10802866
ebirs10802866
HLIrs10802866
Exacrs10802866
Varsomers10802866
Maprs10802866
PheGenIrs10802866
hapmaprs10802866
1000 genomesrs10802866
hgdprs10802866
ensemblrs10802866
gopubmedrs10802866
geneviewrs10802866
scholarrs10802866
googlers10802866
pharmgkbrs10802866
gwascentralrs10802866
openSNPrs10802866
23andMers10802866
23andMe allrs10802866
SNP Nexus

SNPshotrs10802866
SNPdbers10802866
MSV3drs10802866
GWAS Ctlgrs10802866
GMAF0.4307
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs10802866
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.603175
summary