Skip to main content

Table 1 SNPs associated with CHD in genome-wide association studies

From: Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record

SNP

Chr.

Gene

Risk allele

ORs (95% CI)

Risk allele frequency

     

Reported

Observed

rs10757278

9

CDKN2A/2B

G

1.28 (1.22, 1.35)

0.45

0.52

rs599839

1

SORT1

A

1.17 (1.11, 1.22)

0.78

0.78

rs3008621

1

MIA3

G

1.11 (1.04, 1.19)

0.26

NA

rs501120

10

Unknown

T

1.30 (1.12, 1.51)

0.84

0.87

rs9818870

3

MRAS

T

1.15 (1.11, 1.19)

0.15

0.15

rs3184504

12

SH2B3

T

1.13 (1.08, 1.18)

0.39

0.49

rs9982601

21

MRPS6

T

1.20 (1.14, 1.27)

0.13

0.14

rs12526453

6

PHACTR1

C

1.12 (1.08, 1.17)

0.65

0.67

rs6725887

2

WDR12

C

1.17 (1.11, 1.23)

0.14

0.13

rs1122608

19

LDLR

G

1.15 (1.10, 1.21)

0.75

0.77

rs11206510

1

PCSK9

T

1.15 (1.10, 1.21)

0.81

0.82

rs1746048

10

CXCL12

C

1.16 (1.09, 1.24)

0.84

0.87