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Table 2 SNPs analyzed in the CLEAR study.

From: Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease

SNP

Chr

Base Pair

Nearby Gene(s)

Minor (Major) Allele

Change in HDL/LDL per copy of minor allele (mg/dL)

Genotyped/Imputation Accuracyf

rs11206510ab

1

55268627

PCSK9

C (T)

-2.8 LDL

0.55

rs11591147cd

1

55278235

PCSK9

T (G)

-16.4 LDL

Genotyped

rs12740374a

1

109619113

CELSR2-PSRC1-SORT1

T (G)

-7.1 LDL

0.97g

rs646776de

1

109620053

CELSR2-PSRC1-SORT1

G (A)

-4.8 LDL

Genotyped

rs4846914ad

1

228362314

GALNT2

G (A)

-0.7 HDL

Genotyped

rs6754295e

2

21059688

APOB

C (A)

0.9 HDL

Genotyped

rs693bcde

2

21085700

APOB

G (A)

-3.0 LDL

Genotyped

rs7575840c

2

21126995

APOB

T (G)

3.7 LDL

Genotyped

rs515135a

2

21139562

APOB

T (C)

-4.9 LDL

0.90

rs6756629e

2

43918594

ABCG5

A (G)

-4.8 LDL

Genotyped

rs6544713a

2

43927385

ABCG8

T (C)

4.6 LDL

1.00

rs12654264cd

5

74684359

HMGCR

T (A)

2.7 LDL

Genotyped

rs3846662e

5

74686840

HMGCR

G (A)

2.4 LDL

Genotyped

rs3846663a

5

74691482

HMGCR

T (C)

2.1 LDL

0.97h

rs1501908a

5

156330747

TIMD4-HAVCR1

G (C)

-2.1 LDL

0.11

rs12670798c

7

21573877

DNAH11

G (A)

2.7 LDL

0.18

rs328cd

8

19864004

LPL

G (C)

2.9 HDL

Genotyped

rs10096633e

8

19875201

LPL

A (G)

1.9 HDL

0.94i

rs12678919a

8

19888502

LPL

G (A)

3.2 HDL

0.94i

rs2083637e

8

19909455

LPL

G (A)

1.5 HDL

0.45

rs471364a

9

15279578

TCC39B

C (T)

-1.1 HDL

No genotyped SNPs within 200 kb

rs3890182cd

9

106687476

ABCA1

A (G)

-1.1 HDL

Genotyped

rs3905000e

9

106696891

ABCA1

A (G)

-1.6 HDL

0.98j

rs1883025a

9

106704122

ABCA1

T (C)

-1.1 HDL

Genotyped

rs7395662e

11

48475469

MADD-FOLH1

A (G)

1.0 HDL

No genotyped SNPs within 200 kb

rs174547a

11

61327359

FADS1-FADS2-FADS3

C (T)

-1.2 HDL

1.00

rs174570e

11

61353788

FADS1-FADS2-FADS3

A (G)

-3.4 LDL

Genotyped

rs964184a

11

116154127

APOA1-APOC3-APOA4-APOA5

G (C)

-2.3 HDL

1.00

rs2338104ab

12

108379551

MMAB-MVK

C (G)

-1.0 HDL

Genotyped

rs2650000a

12

119873345

HNF1A

A (C)

2.1 LDL

0.98

rs10468017a

15

56465804

LIPC

T (C)

1.4 HDL

0.029

rs1532085e

15

56470658

LIPC

A (G)

1.8 HDL

0.17

rs1800588cd

15

56510967

LIPC

T (C)

1.4 HDL

Genotyped

rs173539a

16

55545545

CETP

T (C)

3.4 HDL

1.00

rs1800775cd

16

55552737

CETP

A (C)

2.5 HDL

Genotyped

rs1532624e

16

55562980

CETP

A (C)

2.9 HDL

Genotyped

rs2271293ae

16

66459571

LCAT-CTCF-PRMT8

A (G)

1.8 HDL

0.98

rs4939883ae

18

45421212

LIPG

A (G)

-1.4 HDL

0.92

rs2967605a

19

8375738

ANGPTL4

T (C)

-1.6 HDL

0.76

rs1529729c

19

11024562

LDLR

C (T)

1.9 LDL

Genotyped

rs6511720abc

19

11063306

LDLR

T (G)

-4.6 LDL

Genotyped

rs2228671e

19

11071912

LDLR

A (G)

-4.2 LDL

Genotyped

rs688c

19

11227602

LDLR

T (C)

1.4 LDL

Genotyped

rs10401969a

19

19268718

NCAN-CILP2-PBX4

C (T)

-1.5 LDL

0.22

rs16996148bd

19

19519472

NCAN-CILP2-PBX4

T (G)

-3.1 LDL

Genotyped

rs157580e

19

50087106

TOMM40-APOE

G (A)

-3.4 LDL

Genotyped

rs2075650e

19

50087459

TOMM40-APOE

G (A)

4.9 LDL

Genotyped

rs4420638abc

19

50114786

APOE

G (A)

8.9 LDL

0.81

rs6102059a

20

38662198

MAFB

T (C)

-1.8 LDL

-0.074

rs1800961a

20

42475778

HNF4A

T (C)

-2.6 HDL

Genotyped

rs7679a

20

44009909

PLTP

C (T)

-1.0 HDL

Genotyped

  1. The estimated changes in HDL or LDL per copy of the minor allele are based on effects reported in aKathiresan et al[14], bWiller CJ et al[15], cKathiresan et al[12], dKathiresan et al[13], and eAulchenko et al[11]. fOnly SNPs with estimated imputation accuracies of >90% were included in downstream analyses. gExcluded from downstream analyses due to r2 = 1.00 with rs646776. hExcluded due to r2 = 0.99 with rs12654264. iExcluded due to r2 = 0.93 and 0.95 with rs328. jExcluded due to r2 = 0.96 with rs3890182.