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Official Journal of the Human Genome Organisation

Table 1 Genome-wide linkage analyses of myocardial infarction (MI), acute coronary syndrome (ACS), or coronary heart disease (CHD)

From: Molecular genetics of myocardial infarction

Chromosomal locus

Marker/gene symbol

Phenotype

References

1p34-p36

D1S1597

MI

Wang et al. (2004)

1q25

D1S518

ACS

Hauser et al. (2004)

2p12-q23.3

D2S2271

CHD

The BHF Family Heart Study Research Group (2005)

2p12-q23.3

D2S2216

MI

The BHF Family Heart Study Research Group (2005)

2q21.1-q22

D2S129, D2S2313

CHD

Pajukanta et al. (2000)

2q36-q37.3

D2S125

ACS

Harrap et al. (2002)

3q13

D3S2460

CHD

Hauser et al. (2004)

3q27

D3S1262, D3S1580

CHD, MI

Francke et al. (2001)

10q23

D10S185

CHD

Francke et al. (2001)

13q12

D13S289/ALOX5AP

MI

Helgadottir et al. (2004)

14q

D14S1426

MI

Broeckel et al. (2002)

15q26

D15S120/MEF2A

CHD, MI

Wang et al. (2003)

16p13-pter

D16S423

CHD

Francke et al. (2001)

17p11.2-q21

D17S921, D17S787

CHD

Farrall et al. (2006)

Xq23-q26

DXS1072, DXS1212

CHD

Pajukanta et al. (2000)