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rs12573606

From SNPedia

Orientationplus
Stabilizedplus
Make rs12573606(A;A)
Make rs12573606(A;G)
Make rs12573606(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position86122545
GeneGRID1
is asnp
is mentioned by
dbSNPrs12573606
ebirs12573606
HLIrs12573606
Exacrs12573606
Varsomers12573606
Maprs12573606
PheGenIrs12573606
hapmaprs12573606
1000 genomesrs12573606
hgdprs12573606
ensemblrs12573606
gopubmedrs12573606
geneviewrs12573606
scholarrs12573606
googlers12573606
pharmgkbrs12573606
gwascentralrs12573606
openSNPrs12573606
23andMers12573606
23andMe allrs12573606
SNP Nexus

SNPshotrs12573606
SNPdbers12573606
MSV3drs12573606
GWAS Ctlgrs12573606
GMAF0.4421
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs12573606
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.539062
summary