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Table 4 Nominally significant single-site associations (P < 0.05) of common SCARB1 variants

From: Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study

SNP Namea

SNP IDb

Chr12 Positionc

Location

Amino Acid Change

RegDB Scored

Major/Minor Alleles

MAF

β

SE

R2 (%)

P

FDR

Secondary Trait (Effect)

Top 3 Variants

HDL-C

              

 p20207

rs11057853

125329313

Intron 1

 

5

G/A

0.4484

0.4082

0.1925

1.0650

0.0343

0.4235

  

 p20741

rs11057851

125328779

Intron 1

 

5

C/T

0.3237

−0.5924

0.2067

1.3010

0.0043

0.1465

ApoA-I (↓)

Top 1

 p45516

rs1902569

125304004

Intron 1

 

5

G/A

0.1544

0.5447

0.2629

0.6390

0.0386

0.4375

  

 p49690

rs4765615

125299830

Intron 2

 

5

G/A

0.4426

−0.4646

0.1866

0.9330

0.0130

0.2526

ApoA-I (↓)

 

 p79828

rs838895

125269692

Intron 11

 

5

C/G

0.3171

0.4961

0.2059

0.8220

0.0162

0.2756

ApoA-I (↑)

 

ApoA-I

              

 p20741

rs11057851

125328779

Intron 1

 

5

C/T

0.3237

−1.2331

0.5117

0.8600

0.0162

0.3186

HDL-C (↓)

 

 p49690

rs4765615

125299830

Intron 2

 

5

G/A

0.4426

−0.9139

0.4614

0.6770

0.0480

0.5022

HDL-C (↓)

 

 p55963

rs7134858

125293557

Intron 6

 

6

C/T

0.1560

1.7537

0.6260

1.0710

0.0052

0.2918

 

Top 2

 p63483

rs838912

125286037

Intron 7

 

7

G/A

0.0867

1.8700

0.8230

0.6880

0.0234

0.3972

  

 p64772

rs5888

125284748

Exon 8

Ala350Ala

3a

C/T

0.0961

2.0962

0.7888

0.9460

0.0080

0.2918

 

Top 3

 p79721

rs838896

125269799

Intron 11

 

5

G/C

0.3104

1.1147

0.5056

0.7270

0.0278

0.4197

  

 p79828

rs838895

125269692

Intron 11

 

5

C/G

0.3171

1.2206

0.5074

0.7800

0.0164

0.3186

HDL-C (↑)

 

 p83884

rs701106

125265636

Intron 12

 

5

C/T

0.2597

1.2967

0.5352

0.7770

0.0156

0.3186

  
  1. ApoA-I apolipoprotein A-I, FDR false discovery rate, HDL-C high-density lipoprotein cholesterol, MAF minor allele frequency, RegDB RegulomeDB, SE standard error, SNP single nucleotide polymorphism, UTR untranslated region, R2, the proportion of the phenotypic variance explained by the variant; ↓, decreased; ↑, increased
  2. Alleles on reverse strand. HDL-C and ApoA-I variables were in mg/dL and Box-Cox transformed
  3. Results were adjusted for covariates: sex, age, waist, current smoking (yes/no), and minutes of walking or biking to work each day (jobmin) for HDL-C; sex and age for ApoA-I
  4. The most significant P-value for each trait is shown in bold, see the single-site association (−log10 P) plot and pairwise correlations (r2) in Fig. 2
  5. FDR that reached a threshold of <0.20 is shown in bold
  6. a, cRefSeq of SCARB1: hg19, NM_005505 (CHIP Bioinformatics)
  7. bdbSNP build 139: GRCh37.p10
  8. dDetailed RegulomeDB (version 1.0) scoring scheme is described in Additional file 17: Table S12 or at http://regulome.stanford.edu/help, see functional assignments in Additional file 18: Table S13