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rs1423901

From SNPedia

Orientationplus
Stabilizedplus
Make rs1423901(A;A)
Make rs1423901(A;G)
Make rs1423901(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position60414548
is asnp
is mentioned by
dbSNPrs1423901
ebirs1423901
HLIrs1423901
Exacrs1423901
Varsomers1423901
Maprs1423901
PheGenIrs1423901
hapmaprs1423901
1000 genomesrs1423901
hgdprs1423901
ensemblrs1423901
gopubmedrs1423901
geneviewrs1423901
scholarrs1423901
googlers1423901
pharmgkbrs1423901
gwascentralrs1423901
openSNPrs1423901
23andMers1423901
23andMe allrs1423901
SNP Nexus

SNPshotrs1423901
SNPdbers1423901
MSV3drs1423901
GWAS Ctlgrs1423901
GMAF0.2796
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1423901
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.710938
summary