Table 1 Global distributions of AIMs.

From: Genetic ancestry plays a central role in population pharmacogenomics

Ancestry groups

VarType

# of SNVs

# of AIMs based on allele-based 2-sided Fisher exact test (the proportion of AIMs, PAIM)

False discovery rate

ALL

MAF = 0

245,462

-

SNP

5,533,074

5,506,536 (99.520%)

RV

58,354,524

7,264,275 (12.449%)

SNP/RV

13,685,123

13,677,393 (99.944%)

Total SNV*

77,572,721

28,531,199 (36.780%)

AFR

MAF = 0

38,873,037

-

SNP

10,326,460

2,530,827 (24.508%)

RV

16,020,578

0 (0%)

SNP/RV

12,598,108

2,711,122 (21.520%)

Total SNV*

38,945,146

3,831,696 (9.839%)

AMR

MAF = 0

51,903,729

-

SNP

7,032,091

3,698,704 (52.597%)

RV

12,632,724

0 (0%)

SNP/RV

6,249,639

459,185 (7.347%)

Total SNV*

25,914,454

3,602,015 (13.900%)

EAS

MAF = 0

56,021,288

-

SNP

6,271,954

1,457,317 (23.235%)

RV

11,680,819

0 (0%)

SNP/RV

3,844,122

750,456 (19.522%)

Total SNV*

21,796,895

1,501,008 (6.886%)

EUR

MAF = 0

55,685,350

-

SNP

7,161,303

854,478 (11.932%)

RV

10,956,920

0 (0%)

SNP/RV

4,014,610

417,108 (10.390%)

Total SNV*

22,132,833

834,331 (3.770%)

SAS

MAF = 0

53,228,676

-

SNP

7,239,212

217,333 (3.002%)

RV

12,766,736

4 (0.000031%)

SNP/RV

4,583,559

187,916 (4.100%)

Total SNV*

24,589,507

172,096 (0.700%)

  1. *Total SNV indicates all polymorphic variants with a nonzero minor allele frequency (MAF), including common variant (SNP), rare variant (RV), and SNP/RV, where 162 variants with duplicated positions were excluded.