Have questions? Visit https://www.reddit.com/r/SNPedia

rs12302525

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs12302525(C;G)
Make rs12302525(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position89332648
is asnp
is mentioned by
dbSNPrs12302525
ebirs12302525
HLIrs12302525
Exacrs12302525
Varsomers12302525
Maprs12302525
PheGenIrs12302525
hapmaprs12302525
1000 genomesrs12302525
hgdprs12302525
ensemblrs12302525
gopubmedrs12302525
geneviewrs12302525
scholarrs12302525
googlers12302525
pharmgkbrs12302525
gwascentralrs12302525
openSNPrs12302525
23andMers12302525
23andMe allrs12302525
SNP Nexus

SNPshotrs12302525
SNPdbers12302525
MSV3drs12302525
GWAS Ctlgrs12302525
GMAF0.1038
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GET Evidence
rs12302525
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.148438
summary