Table 1 GWAS results of the four different analyses

From: Genome-wide association studies of COVID-19 vaccine seroconversion and breakthrough outcomes in UK Biobank

Phenotype

SNP

CHR

BP

EA

OA

EAF

OR

SE

PVAL

Function

Gene/Nearest genes

Seroconversion - One dose

rs9275109

6

32,649,676

T

G

0.61

0.86

0.01

1.1e−26

intergenic

HLA-DQB1 - MTCO3P1

Seroconversion - One dose

rs79510369

2

160,858,048

T

A

0.01

1.48

0.06

5.3e−10

intronic

PLA2R1

Seroconversion - Two dose

rs68033958

6

32,634,226

A

G

0.16

0.82

0.02

1.4e−21

intronic

HLA-DQB1

Seroconversion - Two dose

rs3094055

6

30,332,146

G

C

0.77

0.89

0.02

2.1e−10

upstream

UBQLN1P1

Breakthrough susceptibility

rs73062389

3

45,835,417

A

G

0.06

1.22

0.01

4.0e-56

intronic

SLC6A20

Breakthrough susceptibility

rs16861415

3

186,696,364

C

T

0.08

0.84

0.01

6.8e-55

intronic

ST6GAL1

Breakthrough susceptibility

rs11673136

19

9,007,748

G

A

0.48

1.08

0.01

4.6e-34

intronic

MUC16

Breakthrough susceptibility

rs112313064

19

5,831,724

C

T

0.36

1.06

0.01

1.1e-22

exonic

FUT6

Breakthrough susceptibility

rs681343

19

49,206,462

T

C

0.50

0.95

0.01

1.4e−17

exonic

FUT2

Breakthrough susceptibility

rs1977829

10

111,975,041

A

G

0.18

0.94

0.01

1.4e−12

intronic

MXI1

Breakthrough susceptibility

rs2550250

3

195,500,549

T

C

0.44

1.05

0.01

1.8e−12

intronic

MUC4

Breakthrough susceptibility

rs6676150

1

155,123,837

C

G

0.39

1.04

0.01

2.7e−12

intergenic

HMGN2P18 - KRTCAP2

Breakthrough susceptibility

rs17347644

3

101,547,733

T

C

0.35

0.96

0.01

1.3e-10

intronic

NFKBIZ

Breakthrough susceptibility

rs5117

19

45,418,790

C

T

0.24

0.96

0.01

4.7e-09

intronic

APOC1

Breakthrough severity

rs429358

19

45,411,941

C

T

0.15

1.21

0.03

1.1e-08

exonic

APOE

  1. Top lead independent variants (P-value ≤ 5  ×  10−8, r2 ≤ 0.1 and window = 250 kb) in FUMA are noted. Association was tested by logistic regression in REGENIE.
  2. SNP single nucleotide polymorphism, CHR chromosome, BP Base pair, EAF effect allele frequency, EA effect allele, OA other allele, OR odds ratio, SE standard error, PVAL P value