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Table 2 SNPs involved in significant interactions. Columns from left to right are: SNP identifier, region in which the SNP is located, gene, Frequencies in the cases, frequencies in the controls, ORs and 95 % of confidence interval (CI), nominal p-value and adjusted p-value

From: Identification of epistatic interactions through genome-wide association studies in sporadic medullary and juvenile papillary thyroid carcinomas

Analysis

SNP

Region

Gene

Frequency cases

Frequency controls

OR [95 % CI]

P-value

Adjusted p-value

sMTC

rs4758915

Intronic

CHFR

0.03704

0.02586

1.449 [0.4003–5.243]

0.5702

0.9812

sMTC

rs10402530

Downstream

AC016582.2

0.1944

0.1897

1.031 [0.5782–1.84]

0.9167

0.9936

sMTC

rs7835921

Intronic

C8orf37

0.4519

0.5086

0.7966 [0.5008–1.267]

0.3365

0.9669

sMTC

rs1287079

Downstream

RNU1-55P

0.3019

0.3664

0.7479 [0.4567–1.225]

0.2476

0.9569

jPTC

rs2235544

Intronic

DIO1

0.4667

0.5043

0.86 [0.487–1.519]

0.6032

0.9696

jPTC

rs16876356

Intronic

DMGDH

0.1167

0.2308

0.4403 [0.1891–1.025]

0.0518

0.9007

jPTC

rs17716031

Intronic

RP11-648K4.2

0.1034

0.1336

0.7481 [0.2964–1.888]

0.5379

0.9668

jPTC

rs10775207

Intronic

LOXL1

0.0167

0.0087

1.932 [0.1723–21.67]

0.5868

0.9668