Table 1 14 independent genetic variants related to the type 2 dibaetes_prs (P < 5 × 10− 8).

From: Pathway insights and predictive modeling for type 2 diabetes using polygenic risk scores

rsID

Gene

Chr.

hg38

Risk

allele

OR

(95% CI)

P value

INFO R2

rs1337028053

--

5

106112143

A

2.97 (2.02–4.37)

2.98E-08

0.7

rs9356744

CDKAL1

6

20685255

C

1.13 (1.09–1.16)

1.38E-14

--

rs1431838560

--

7

109778774

C

2.32 (1.74–3.10)

1.25E-08

0.97

rs806214

FSCN3

7

127596949

A

0.90 (0.87–0.93)

1.20E-10

0.99

rs2233580

PAX4

7

127613496

T

1.26 (1.21–1.32)

1.67E-24

--

rs201976370

SND1

7

127969728

A

1.26 (1.20–1.32)

1.54E-22

0.96

rs10811661

CDKN2B-AS1;DMRTA1

9

22134095

T

0.88 (0.85–0.91)

1.26E-16

--

rs2283228

KCNQ1

11

2828300

A

0.88 (0.85–0.91)

1.19E-15

--

rs2237895

KCNQ1

11

2835964

C

1.18 (1.15–1.22)

5.81E-28

--

rs17676332

TYRO3

15

41567301

T

1.32 (1.22–1.43)

1.34E-12

--

rs76072851

CORO2B

15

68640950

T

1.72 (1.62–1.82)

8.31E-74

--

rs527631646

LINC01582;LINC02351

15

98177053

C

2.50 (1.82–3.43)

1.73E-08

0.6

rs551262605

PSMD3

17

39984855

A

3.13 (2.08–4.72)

4.50E-08

0.72

rs148612115

ZNF257

19

22089299

T

0.79 (0.74–0.85)

1.92E-11

0.96

  1. Chr, chromosome; hg38, Homo sapiens (human) genome assembly GRCh38; OR, odds ratio; CI, confidence interval.