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rs9806699

From SNPedia

Orientationplus
Stabilizedplus
Make rs9806699(A;A)
Make rs9806699(A;G)
Make rs9806699(G;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position45448194
is asnp
is mentioned by
dbSNPrs9806699
ebirs9806699
HLIrs9806699
Exacrs9806699
Varsomers9806699
Maprs9806699
PheGenIrs9806699
hapmaprs9806699
1000 genomesrs9806699
hgdprs9806699
ensemblrs9806699
gopubmedrs9806699
geneviewrs9806699
scholarrs9806699
googlers9806699
pharmgkbrs9806699
gwascentralrs9806699
openSNPrs9806699
23andMers9806699
23andMe allrs9806699
SNP Nexus

SNPshotrs9806699
SNPdbers9806699
MSV3drs9806699
GWAS Ctlgrs9806699
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 25863251] GATM Polymorphism Associated with the Risk for Statin-Induced Myopathy Does Not Replicate in Case-Control Analysis of 715 Dyslipidemic Individuals