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rs463426

From SNPedia

Orientationplus
Stabilizedplus
Make rs463426(C;C)
Make rs463426(C;T)
Make rs463426(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position21454896
is asnp
is mentioned by
dbSNPrs463426
ebirs463426
HLIrs463426
Exacrs463426
Varsomers463426
Maprs463426
PheGenIrs463426
hapmaprs463426
1000 genomesrs463426
hgdprs463426
ensemblrs463426
gopubmedrs463426
geneviewrs463426
scholarrs463426
googlers463426
pharmgkbrs463426
gwascentralrs463426
openSNPrs463426
23andMers463426
23andMe allrs463426
SNP Nexus

SNPshotrs463426
SNPdbers463426
MSV3drs463426
GWAS Ctlgrs463426
GMAF0.4385
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs463426
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.625
summary