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Table 1 SNPs detected by sequencing the LXRβ gene.

From: Suggestive evidence of associations between liver X receptor β polymorphisms with type 2 diabetes mellitus and obesity in three cohort studies: HUNT2 (Norway), MONICA (France) and HELENA (Europe)

#

rs number

Position on chromosome 19

Position from ATG

Location

Base change

MAF in sequenced individuals

(n = 96)

MAF in HUNT2 controls

(n = 1986)

MAF in MONICA

(n = 2318)

MAF in HELENA-CSS

(n = 1144)

1

rs79233036a

55,569,984

-2692

5' near gene

C>T

0.005 (1 heterozygous subject)

0

-

-

2

rs77094157a

55,570,236

-2440

5' near gene

C>T

0.005 (1 heterozygous subject)

NA

-

-

3

rs12972221

55,570,952

-1723

5' near gene

G>T

0.36

NA

-

-

4

rs17373080

55,571,336

-1339

5' near gene

C>G

0.37

0.35

0.31

0.32

5

rs56151148

55,571,364

-1311

5' near gene

C>T

0.05

0.08

0.09

0.08

6

rs55794952

55,571,487

-1188

5' near gene

G>T

0.005 (1 heterozygous subject)

0.007

-

-

7

rs2695121

55,572,553

-122

intron 2

C>T

0.44

0.44

0.43

0.40

8

rs55671147

55,572,866

+192

exon 4

G>A (Glu36Glu)

0.03

NA

-

-

9

rs28514894

55,573,138

+464

intron 4

C>T

0.33

0.35

-

-

10

rs2248949

55,573,981

+1306

intron 6

G>A

0.45

0.44

-

-

11

rs41432149

55,573,984

+1309

intron 6

C>T

0.36

0.35

-

-

12

rs77290536a

55,574,080

+1405

exon 7

C>G (Pro252Arg)

0.005 (1 heterozygous subject)

0

-

-

13

rs78105260a

55,574,374

+1700

intron 7

A>G

0.005 (1 heterozygous subject)

0.007

-

-

14

rs1405655

55,574,431

+1757

intron 7

C>T

0.36

0.35

-

-

15

rs2303045

55,574,730

+2056

intron 7

C>G

0.35

0.35

-

-

16

rs4802703

55,576,697

+4023

intron 8

A>C

0.40

0.32

-

-

17

rs2303044

55,577,013

+4339

intron 8

A>G

0.10

0.07

0.08

0.08

18

rs1052677

55,577,993

+5319

3' UTR

C>G

0.16

0.09

-

-

19

rs75967835a

55,578,378

+5704

3' near gene

A>C

0.005 (1 heterozygous subject)

0

-

-

20

rs3219281

55,578,899

+6225

3' near gene

C>T

0.15

0.09

0.09

0.10

  1. Positions based on NM_007121 sequence. MAF: minor allele frequency. NA: not available.
  2. The 5 SNPs selected for association studies are indicated in bold.
  3. adiscovered by gene sequencing in the present study.