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rs446112

From SNPedia

Orientationplus
Stabilizedplus
Make rs446112(A;A)
Make rs446112(A;G)
Make rs446112(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position46448270
is asnp
is mentioned by
dbSNPrs446112
ebirs446112
HLIrs446112
Exacrs446112
Varsomers446112
Maprs446112
PheGenIrs446112
hapmaprs446112
1000 genomesrs446112
hgdprs446112
ensemblrs446112
gopubmedrs446112
geneviewrs446112
scholarrs446112
googlers446112
pharmgkbrs446112
gwascentralrs446112
openSNPrs446112
23andMers446112
23andMe allrs446112
SNP Nexus

SNPshotrs446112
SNPdbers446112
MSV3drs446112
GWAS Ctlgrs446112
GMAF0.3939
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs446112
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.5
summary