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Table 2 Distribution of SNPs of Numb gene for study population

From: Genetic variants of numb gene were associated with elevated total cholesterol level and low density lipoprotein cholesterol level in Chinese subjects, in Xinjiang, China

Varients

 

Total N (%)

Male N (%)

Female N (%)

P value

rs2108552 (SNP1)

Genotype

C/C

281 (17.0)

174 (16.5)

107 (18.0)

0.732

 

G/G

568 (34.4)

367 (34.8)

201 (33.7)

 
 

C/G

799 (48.6)

511 (48.7)

288 (48.3)

 

Dominant model

CC

281 (17.0)

174 (16.5)

107 (18.0)

0.464

 

CG + GG

1367 (83.0)

878 (83.5)

489 (82.0)

 

Recessive model

GG

568 (34.4)

367 (34.8)

201 (33.7)

0.634

 

CG + CC

1080 (65.6)

685 (65.2)

395 (66.3)

 

Additive model

CG

799 (48.6)

511 (48.7)

288 (48.3)

0.922

 

CC + GG

849 (51.4)

541 (51.3)

308 (51.7)

 

Allele

C

1361 (41.3)

859 (40.8)

502 (42.1)

0.471

 

G

1935 (58.7)

1245 (59.2)

690 (57.9)

 

rs12435797 (SNP2)

Genotype

T/T

532 (32.3)

323 (30.7)

209 (35.1)

0.111

 

G/G

348 (21.1)

235 (22.3)

113 (19.0)

 
 

G/T

768 (46.6)

495 (47.0)

273 (45.9)

 

Dominant model

TT

532 (32.3)

323 (30.7)

209 (35.1)

0.063

 

GT + GG

1116 (67.7)

730 (69.3)

386 (64.9)

 

Recessive model

GG

348 (21.1)

235 (22.3)

113 (19.0)

0.112

 

GT + TT

1300 (78.9)

818 (77.7)

482 (81.0)

 

Additive model

GT

768 (46.6)

495 (47.0)

273 (45.9)

0.660

 

TT + GG

880 (53.4)

558 (53.0)

322 (54.1)

 

Allele

T

1832 (55.6)

1141 (54.2)

691 (58.1)

0.031*

 

G

1464 (44.4)

965 (45.8)

499 (41.9)

 

rs1019075 (SNP3)

Genotype

C/C

176 (10.7)

115 (10.9)

61 (10.2)

0.846

 

T/T

848 (51.5)

536 (51.0)

312 (52.3)

 
 

C/T

624 (37.9)

401 (38.1)

223 (37.4)

 

Dominant model

CC

176 (10.7)

115 (10.9)

61 (10.2)

0.660

 

CT + TT

1472 (89.3)

937 (89.1)

535 (89.8)

 

Recessive model

TT

848 (51.5)

536 (51.0)

312 (52.3)

0.585

 

CT + CC

800 (48.5)

516 (49.0)

284 (47.7)

 

Additive model

CT

624 (37.9)

401 (38.1)

223 (37.4)

0.778

 

CC + TT

1024 (62.1)

651 (61.9)

373 (62.6)

 

Allele

C

976 (29.6)

631 (30.0)

345 (28.9)

0.527

 

T

2320 (70.4)

1473 (70.0)

847 (71.1)

 

rs17781919 (SNP4)

Genotype

C/C

1621 (98.4)

1034 (98.0)

587 (99.0)

0.133

 

C/T

27 (1.6)

21 (2.0)

6 (1.0)

 

Allele

C

3269 (99.2)

2089 (99.0)

1180 (99.5)

0.135

 

T

27 (0.8)

21 (1.0)

6 (0.5)

 
  1. The P value of genotype was calculated by Fisher’s exact test
  2. *P <0.05