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rs456210

From SNPedia

Orientationplus
Stabilizedplus
Make rs456210(A;A)
Make rs456210(A;G)
Make rs456210(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position46453332
is asnp
is mentioned by
dbSNPrs456210
ebirs456210
HLIrs456210
Exacrs456210
Varsomers456210
Maprs456210
PheGenIrs456210
hapmaprs456210
1000 genomesrs456210
hgdprs456210
ensemblrs456210
gopubmedrs456210
geneviewrs456210
scholarrs456210
googlers456210
pharmgkbrs456210
gwascentralrs456210
openSNPrs456210
23andMers456210
23andMe allrs456210
SNP Nexus

SNPshotrs456210
SNPdbers456210
MSV3drs456210
GWAS Ctlgrs456210
GMAF0.3926
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs456210
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.5
summary