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rs1110866

From SNPedia

Orientationplus
Stabilizedplus
Make rs1110866(A;A)
Make rs1110866(A;C)
Make rs1110866(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position56792296
GeneARHGEF3
is asnp
is mentioned by
dbSNPrs1110866
ebirs1110866
HLIrs1110866
Exacrs1110866
Varsomers1110866
Maprs1110866
PheGenIrs1110866
hapmaprs1110866
1000 genomesrs1110866
hgdprs1110866
ensemblrs1110866
gopubmedrs1110866
geneviewrs1110866
scholarrs1110866
googlers1110866
pharmgkbrs1110866
gwascentralrs1110866
openSNPrs1110866
23andMers1110866
23andMe allrs1110866
SNP Nexus

SNPshotrs1110866
SNPdbers1110866
MSV3drs1110866
GWAS Ctlgrs1110866
GMAF0.3476
Max Magnitude
? (A;A) (A;C) (C;C) 28


GET Evidence
rs1110866
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.320312
summary