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. 2016 May 9;6:25614. doi: 10.1038/srep25614

Table 7. The 17 SNVs significantly different between case and control.

Gene Chr Pos Ref Obs caseRef caseAlt controlRef controlAlt FisherExactTestPvalue Sanger sequencing validated
PPARG chr3 12475632 G A 15 1 1600 0 0.00990099 No
CPT2 chr1 53679028 G A 15 1 1599 1 0.019710021 Yes
FCGR2A chr1 161479745 A G 13 3 836 764 0.023221855 Yes
RPAIN chr17 5326145 C G 2 14 638 962 0.036500478 Yes
TLR3 chr4 187004074 C T 6 10 1069 531 0.028998842 Yes
NOS3 chr7 150704250 C G 12 4 785 815 0.04531093 Yes
ABCB1 chr7 87179601 A G 13 3 862 738 0.040826503 Yes
LEP chr7 127892124 A G 15 1 1597 3 0.039055387 Yes
TLR4 chr9 120470894 C G 15 1 1600 0 0.00990099 Yes
KLRC2 chr12 10587111 A G 3 13 923 677 0.003533467 Yes
chr12 10588530 C G 14 2 835 765 0.004729536 Yes
CES1 chr16 55844509 T C 15 1 1600 0 0.00990099 Yes
DNMT1 chr19 10265312 T C 0 16 433 1167 0.00938611 Yes
chr19 10265333 A G 15 1 1600 0 0.00990099 Yes
chr19 10265372 C T 15 1 1600 0 0.00990099 Yes
MX1 chr21 42817930 G A 15 1 885 715 0.001564732 Yes
chr21 42824661 A G 12 4 766 834 0.042066821 Yes