The association of genetic polymorphisms in interleukin-1 receptors type 1 and type 2 with sudden sensorineural hearing loss in a Taiwanese population: a case control study

Table 3. The association between IL1R SNP rs2234650 under recessive model, and rs4141134 under dominant model with SSNHL

SNP	Case n (%)	Control, n (%)	Adjusted OR (95% CI)^b, P value^a
rs2234650 Recessive
Genotypes
CC + CT	358 (89%)	691 (95%)	1.00^c
TT	43 (11%)	39 (5%)	2.681 (1.17–5.95), P = 0.0206*
rs4141134 Dominant
Genotypes
TT	318 (79%)	679 (93%)	1.00^c
CC + CT	83 (21%)	51 (7%)	4.087 (2.14–7.83), P < 0.0001*

ISSN: 1916-0216