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rs2404646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2404646(C;G)
Make rs2404646(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position135165126
is asnp
is mentioned by
dbSNPrs2404646
ebirs2404646
HLIrs2404646
Exacrs2404646
Varsomers2404646
Maprs2404646
PheGenIrs2404646
hapmaprs2404646
1000 genomesrs2404646
hgdprs2404646
ensemblrs2404646
gopubmedrs2404646
geneviewrs2404646
scholarrs2404646
googlers2404646
pharmgkbrs2404646
gwascentralrs2404646
openSNPrs2404646
23andMers2404646
23andMe allrs2404646
SNP Nexus

SNPshotrs2404646
SNPdbers2404646
MSV3drs2404646
GWAS Ctlgrs2404646
GMAF0.1492
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs2404646
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.171875
summary