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Table 2 Significant hits from association

From: Application of next generation sequencing to CEPH cell lines to discover variants associated with FDA approved chemotherapeutics

Drug(s)

SNP ID

SNP position

Gene

q-value

MAF

Arsenic Trioxide

rs60900828 (A/T)

Chr16:56671632

MT1A (near-gene 5)

0.047628

0.138

Oxaliplatin

rs562 (C/T)

Chr3:183637845

ABCC5 (UTR3)

0.049494

0.392

 

rs3749445 (A/G)

Chr3:183638506

ABCC5 (UTR3)

0.044895

0.410

 

rs2292998 (C/T)

Chr3:183663833

ABCC5 (intronic)

0.039882

0.277

 

rs1016752 (C/G)

Chr3:183665062

ABCC5 (intronic)

0.039781

0.232

 

rs4148585 (C/T)

Chr3:183670642

ABCC5 (intronic)

0.039781

0.283

 

rs6443924 (A/G)

Chr3:183679532

ABCC5 (intronic)

0.039781

0.279

 

rs4148579 (A/G)

Chr3:183685249

ABCC5 (intronic)

0.039781

0.279

 

rs939336 (A/G => C594C)

Chr3:183685534

ABCC5 (exonic)

0.039781

0.279

 

rs1132776 (C/T => A395A)

Chr3:183696402

ABCC5 (exonic)

0.044895

0.289

 

rs2313212 (C/T)

Chr3:183700928

ABCC5 (intronic)

0.039781

0.279

 

rs4148575 (C/T)

Chr3:183702275

ABCC5 (UTR3)

0.044895

0.289

 

rs1846692 (C/T)

Chr16:56671696

MT1A (near - gene 5)

0.049494

0.360

 

rs35346959 (A/G)

Chr16:56671867

MT1A (near- gene 5)

0.044895

0.137

 

rs9922957 (C/G)

Chr16:56672380

MT1A (near - gene 5)

0.039781

0.185

 

rs9922409 (A/G)

Chr16:56672400

MT1A (near - gene 5)

0.04532

0.103

 

rs7190725 (G/T)

Chr16:56673290

MT1A (intronic)

0.044895

0.170

 

rs8052394 (A/G => K51R)

Chr16:56673828

MT1A (missense)

0.044895

0.152

 

rs1800566 (C/T => P187S)

chr16:69745145

NQO1 (exonic)

0.039781

0.258

 

rs689455 (A/C)

Chr16:69761661

NQO1 (near- gene 5)

0.039781

0.242

  1. Significant hits from association at FDR corrected threshold of 0.05 are shown in this table. All hits are known dbSNP common variants. All data is reported from Database of Single Nucleotide Polymorphisms (build 137).