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Table 3 Details of the replicated loci both from published studies, replication cohort and strongest signal in the region

From: Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients

Reference

Locus

Published SNP

Strongest signal in the locus (current study)

Position (hg38)

Risk allele

Published studies

Replication

Effect size (OR/HR)

P-value

Medication

Association OR

P-value

Imputation Info

Diouf

14q21.1

rs8014839

 

39,374,915

G

3.63

5.1 × 10−6

Vincristine

1.55

0.0006

0.99

   

rs8014839a

39,374,915

G

 

NA

NA

NA

Diouf

4q28.1

rs4618330

 

126,757,231

A

0.47

6.4 × 10− 6

Vincristine

0.7

0.004

0.98

   

rs28742896 c

127,678,685

A

 

0.6

0.0001

0.99

Baldwin

3q27.3

rs1903216

 

187,911,715

A

1.59

5.6 × 10−6

Paclitaxel

1.4

0.006

1

   

rs2611620 c

187,826,512

A

 

1.69

5.6 × 10−5

0.98

Diouf

3p14.2

rs35558909

 

60,933,303

G

3.17

4.3 × 10−7

Vincristine

1.36

0.01

0.98

   

rs2121845 a

60,922,227

A

 

1.76

0.01

1

Diouf

3p21.1

rs4687753

 

53,861,434

A

4.49

6.2 × 10−6

Vincristine

1.32

0.03

0.99

   

rs9840079b

53,858,614

T

 

1.39

0.007

0.99

Diouf

8q24.12

rs7817522

 

120,028,312

T

4.21

3.1 × 10−6

Vincristine

1.3

0.03

0.99

   

rs17822044a

119,997,585

G

 

1.35

0.02

1

Schneider

15q21.3

rs2062640

 

54,737,776

G

2.01

7.9 × 10− 6

Paclitaxel

1.42

0.04

1

   

rs2695677 c

54,799,953

C

 

1.96

0.0003

0.98

Diouf

2q33.3

rs11694118

 

208,077,000

A

0.18

8.8 × 10−6

Vincristine

0.75

0.04

0.96

   

rs17538082a

208,060,995

T

 

0.73

0.03

1

Diouf

5q23.2

rs10070183

 

124,521,298

C

0.43

2.8 × 10− 6

Vincristine

0.77

0.04

0.95

   

rs10478625b

124,527,954

T

 

0.71

0.009

1

  1. Chr Chromosome, SNP Single nucleotide polymorphism, OR Odds ratio, HR Hazard ratio, NA: not applicable
  2. ar2 ≥ 0.8, b r2 ≥ 0.6, c r2 ≥ 0.4 (r2: The linkage disequilibrium metrics between the SNPs), Imputation Info: the score ranging between 0 and 1 which is the indicator of the certainty of imputation for each SNP