Table 2 Lead variants from 1KG+7K mapping outside previously reported loci (Kanai et al., 2018) not significant in TOPMed

From: Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population

Serum uric acid levels

Locus

Chr

rs ID

Position

Major allele

Minor allele

Imputation up to TOPMed panel

Imputation up to 1KG+7K panel

MAF

Beta

SE

p-value

r2

MAF

Beta

SE

p-value

r2

SRGAP2-AS1/LINC02798

1

rs1156692814

121,432,234

G

C

NA

NA

NA

NA

NA

0.0092

–0.1746

0.0320

4.9.E–08

0.494

SLC22A13

3

rs117371763

38,317,479

C

T

0.0261

–0.0748

0.0148

4.2E–07

0.833

0.0483

–0.0667

0.0105

1.8.E–10

0.921

PSORS1C1/PSORS1C2

6

rs2233950

31,106,065

C

T

0.0462

–0.0510

0.0103

8.0E–07

0.982

0.0412

–0.0611

0.0108

1.4.E–08

1.000

MAP7

6

rs78302547

136,860,353

A

C

NA

NA

NA

NA

NA

0.0071

–0.1704

0.0299

1.3.E–08

0.730

NRG4

15

rs12595289

76,251,105

G

A

0.1534

–0.0257

0.0066

1.0.E–04

0.814

0.1750

–0.0381

0.0061

5.0.E–10

0.852

Total Cholesterol Levels

Locus

Chr

rs ID

Position

Major allele

Minor allele

Imputation up to TOPMed panel

Imputation up to 1KG+7K panel

MAF

Beta

SE

p-value

r2

MAF

Beta

SE

p-value

r2

PPIA/H2AZ2

7

rs899749693

44,862,003

C

A

NA

NA

NA

NA

NA

0.0023

–0.2622

0.0441

2.7E–09

0.873

  1. Chr chromosome, MAF minor allele frequency, SE standard error, Effect effect of the minor allele.