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

rs12257526

From SNPedia

Orientationplus
Stabilizedplus
Make rs12257526(C;C)
Make rs12257526(C;T)
Make rs12257526(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position86169086
GeneGRID1
is asnp
is mentioned by
dbSNPrs12257526
ebirs12257526
HLIrs12257526
Exacrs12257526
Varsomers12257526
Maprs12257526
PheGenIrs12257526
hapmaprs12257526
1000 genomesrs12257526
hgdprs12257526
ensemblrs12257526
gopubmedrs12257526
geneviewrs12257526
scholarrs12257526
googlers12257526
pharmgkbrs12257526
gwascentralrs12257526
openSNPrs12257526
23andMers12257526
23andMe allrs12257526
SNP Nexus

SNPshotrs12257526
SNPdbers12257526
MSV3drs12257526
GWAS Ctlgrs12257526
GMAF0.1965
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs12257526
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.210938
summary