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Table 4 Significant allelic association of SNPs at 11q23.3 chromosomal region with dyslipidemia: Odds ratios from logistic regression of dyslipidemia on variant alleles, before and after adjusting for age, sex and BMI

From: Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India

SNP ID

Gene/Functional relevance

Alleles

Minor/Major

Minor Allele Frequency

Unadjusted

Adjusted for Age, Sex and BMI

Cases

Controls

OR

p-value

OR

p-value

rs17440396

BUD13/Intronic

A/G

0.24

0.18

1.4(1.04–1.98)

0.025

1.5(1.08–2.18)

0.015

rs10488699

A/G

0.23

0.17

1.4(1.03–1.98)

0.031

1.5(1.04–2.03)

0.029

rs2187126a

G/A

0.19

0.09

2.2(1.50–3.25)

4.07 × 10−5

2.3(1.52–3.41)

6.04 × 10−5

rs6589566

ZPR1/Intronic

G/A

0.20

0.29

0.6(0.46–0.86)

0.003

0.7(0.5–0.91)

0.009

rs633389a

APOA5-A4/Intergenic

T/C

0.22

0.12

2.1(1.47–3.02)

3.72 × 10−5

2.0(1.41–2.87)

0.0001

rs672143

G/A

0.00

0.03

0.1(0.01–0.63)

0.002

0.1(0.01–0.72)

0.022

rs1263163a

A/G

0.30

0.14

2.6(1.86–3.57)

7.16 × 10−9

3.1(2.15–4.52)

2.19 × 10−9

rs1263171

A/G

0.48

0.40

1.4(1.07–1.82)

0.013

1.3(1.03–1.72)

0.024

rs2854116

APOC3/upstream 2 kb

A/G

0.40

0.48

0.7(0.54–0.97)

0.032

0.7(0.56–0.98)

0.038

rs632153

APOA1/upstream 2 kb

T/G

0.04

0.02

2.2(1.04–4.84)

0.035

2.4(1.08–5.22)

0.030

  1. Bold indicates risk increasing nature of the minor allele
  2. aSignificant after correction for multiple testing