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Table 1 Genotype and allele frequencies of the rs6679677, rs17696736 and rs763361 SNPs in the type 1 diabetes patients and control subjects.

From: Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population

SNP

(Gene region)

Cases (%)

(N = 154)

Control(%)

(N = 230)

Odds ratio (95%CI)

P

rs6679677

(PHTF1-PTPN22)

    

AA

13(8.4)

6(2.6)

4.23(1.56-11.52)

0.0047

AC

53(34.5)

52(22.6)

1.99(1.26-3.16)

0.0034

CC

88(57.1)

172(74.8)

1*

 

A

79(25.6)

64(13.9)

2.13(1.48-3.08)

0.00001

C

229(74.4)

396(86.1)

1*

 

rs17696736

(C12orf30)

    

AA

38(24.7)

88(38.3)

1*

 

AG

83(53.9)

109(47.4)

1.76(1.10-2.84)

0.0194

GG

33(21.4)

33(14.3)

2.32(1.25-4.28)

0.0074

A

159(51.6)

285(61.9)

1*

 

G

149(48.4)

175(38.1)

1.53(1.14-2.04)

0.0046

rs763361

(CD226)

    

CC

36(23.4)

76(33.1)

1*

 

CT

79(51.3)

118(51.3)

1.41(0.87-2.30)

0.16

TT

39(25.3)

36(15.6)

2.29(1.25-4.18)

0.0071

C

151(49.1)

270(58.7)

1*

 

T

157(50.9)

190(41.3)

1.48(1.11-1.98)

0.0084

  1. 1*: referent estimate