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Table 4 Genome-wide significant loci by cross-trait meta-analysis at sentinel SNPs associated with COPD and CAD (Pmeta < 5 × 10−8; single trait P < 0.01)

From: Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis

Sentinel SNP

CHR

N

Position

P CAD

P COPD

P META

Variant annotation

Genes within clumping region

rs2128739

11

13

chr11:103660567–103,718,660

7.05 × 10−11

3.69 × 10−3

3.17 × 10−12

Intergenic

RP11-563P16.1

rs8046697

16

164

chr16:75236763–75,516,534

3.24 × 10−6

8.1 × 10−4

3.80 × 10−8

Intron

BCAR1, CFDP1, CHST6, CTRB1, CTRB2, LOC100506281, TMEM170A

rs8108474

19

27

chr19:46190268–46,370,381

7.51 × 10−6

5.62 × 10−5

1.49 × 10−8

Intron

DMPK, DMWD, FBXO46, FOXA3, LOC388553, QPCTL, RSPH6A, SIX5, SNRPD2, SYMPK

  1. SNP single nucleotide polymorphisms, CHR chromosome, CAD coronary artery disease, COPD chronic obstructive pulmonary disease