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rs1012620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1012620(A;G)
Make rs1012620(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position40761921
is asnp
is mentioned by
dbSNPrs1012620
ebirs1012620
HLIrs1012620
Exacrs1012620
Varsomers1012620
Maprs1012620
PheGenIrs1012620
hapmaprs1012620
1000 genomesrs1012620
hgdprs1012620
ensemblrs1012620
gopubmedrs1012620
geneviewrs1012620
scholarrs1012620
googlers1012620
pharmgkbrs1012620
gwascentralrs1012620
openSNPrs1012620
23andMers1012620
23andMe allrs1012620
SNP Nexus

SNPshotrs1012620
SNPdbers1012620
MSV3drs1012620
GWAS Ctlgrs1012620
GMAF0.1253
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1012620
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.109375
summary