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rs2676527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2676527(C;G)
Make rs2676527(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position172882984
GeneRAPGEF4
is asnp
is mentioned by
dbSNPrs2676527
ebirs2676527
HLIrs2676527
Exacrs2676527
Varsomers2676527
Maprs2676527
PheGenIrs2676527
hapmaprs2676527
1000 genomesrs2676527
hgdprs2676527
ensemblrs2676527
gopubmedrs2676527
geneviewrs2676527
scholarrs2676527
googlers2676527
pharmgkbrs2676527
gwascentralrs2676527
openSNPrs2676527
23andMers2676527
23andMe allrs2676527
SNP Nexus

SNPshotrs2676527
SNPdbers2676527
MSV3drs2676527
GWAS Ctlgrs2676527
GMAF0.02801
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs2676527
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.960317
summary