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rs10403955
|
CYP2B6
|
Intronic CYP2B6 haplotype-tagging variant associated with altered plasma conc...
|
Pharmacogenomics
|
|
Moderate
|
|
rs1057910
|
CYP2C9
*3
|
No-function CYP2C9 variant with major warfarin implications
|
Pharmacogenomics
|
|
Established
|
|
rs1058164
|
CYP2D6
|
Synonymous CYP2D6 variant that promotes exon 3 skipping, reducing functional ...
|
Pharmacogenomics
|
|
Moderate
|
|
rs1065852
|
CYP2D6
*10
|
Decreased function CYP2D6 variant common in Asian populations
|
Pharmacogenomics
|
|
Established
|
|
rs1080985
|
CYP2D6
*2A promoter
|
CYP2D6 promoter variant (-1584C>G) that reduces enzyme expression; the C alle...
|
Pharmacogenomics
|
|
Strong
|
|
rs1113129
|
CYP2C8
|
Intronic tagging SNP for CYP2C8 haplotype C, a low-activity haplotype associa...
|
Pharmacogenomics
|
|
Moderate
|
|
rs16947
|
CYP2D6
*2
|
Common CYP2D6 variant defining the *2 allele; previously considered normal-fu...
|
Pharmacogenomics
|
|
Strong
|
|
rs17002852
|
CYP2D6
|
Synonymous CYP2D6 variant that causes allele dropout in standard CYP2D6*3 gen...
|
Pharmacogenomics
|
|
Moderate
|
|
rs1799853
|
CYP2C9
*2
|
Decreased function variant affecting warfarin, phenytoin, and NSAIDs
|
Pharmacogenomics
|
|
Established
|
|
rs1799971
|
OPRM1
A118G
|
Mu-opioid receptor variant affecting opioid response, pain sensitivity, and p...
|
Pharmacogenomics
|
|
Strong
|
|
rs1934963
|
CYP2C9
|
Deep intronic CYP2C9 variant associated with altered drug response to sulfony...
|
Pharmacogenomics
|
|
Emerging
|
|
rs1934967
|
CYP2C9
|
Intronic CYP2C9 haplotype tag associated with altered warfarin sensitivity an...
|
Pharmacogenomics
|
|
Moderate
|
|
rs2246709
|
CYP3A4
|
Intronic CYP3A4 variant associated with altered drug clearance, affecting met...
|
Pharmacogenomics
|
|
Moderate
|
|
rs28371706
|
CYP2D6
*17
|
Decreased-function CYP2D6 allele common in African populations, reducing meta...
|
Pharmacogenomics
|
|
Established
|
|
rs28371725
|
CYP2D6
*41
|
Intronic splice variant causing decreased CYP2D6 enzyme activity through aber...
|
Pharmacogenomics
|
|
Established
|
|
rs28371733
|
CYP2D6
|
Rare CYP2D6 stop-gain variant (Glu418Ter) that eliminates enzyme activity, ca...
|
Pharmacogenomics
|
|
Established
|
|
rs28695233
|
CYP2D6
|
Deep intronic CYP2D6 variant in intron 2 that serves as a haplotype tag in sp...
|
Pharmacogenomics
|
|
Emerging
|
|
rs373489637
|
CYP2B6
V183G
|
Near-complete loss-of-function CYP2B6 variant causing severely impaired metab...
|
Pharmacogenomics
|
|
Moderate
|
|
rs3745274
|
CYP2B6
516G>T
|
Decreased-function variant affecting metabolism of efavirenz, methadone, bupr...
|
Pharmacogenomics
|
|
Established
|
|
rs3892097
|
CYP2D6
*4
|
CYP2D6 *4 splice-defect null allele — the most common loss-of-function CYP2D6...
|
Pharmacogenomics
|
|
Established
|
|
rs5030655
|
CYP2D6
*6
|
Frameshift deletion causing no enzyme function, defining poor metabolizer sta...
|
Pharmacogenomics
|
|
Established
|
|
rs58440431
|
CYP2D6
|
Intronic CYP2D6 variant tagging East Asian *10-lineage suballeles; the C alle...
|
Pharmacogenomics
|
|
Strong
|
|
rs640561
|
LRRIQ3
|
Intergenic variant near LRRIQ3 associated with problematic opioid prescriptio...
|
Pharmacogenomics
|
|
Emerging
|
|
rs67807361
|
CYP2C9
p.Leu19Ile
|
Rare CYP2C9 N-terminal missense variant of uncertain functional significance ...
|
Pharmacogenomics
|
|
Emerging
|
|
rs71328650
|
CYP2D6
|
Intronic CYP2D6 haplotype tag variant (rs28371702 canonical form) associated ...
|
Pharmacogenomics
|
|
Emerging
|
|
rs72549354
|
CYP2D6
*20
|
Frameshift insertion creating a null CYP2D6 allele; carriers cannot metaboliz...
|
Pharmacogenomics
|
|
Established
|