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. 2020 Jun 24;10:10236. doi: 10.1038/s41598-020-66951-5

Table 1.

Summary of the CD-GWAS results in Japanese patients.

Chr Range (bp)* Top Hit SNP No. of SNPs** Genes
From To SNP ID Position* A1 A2 A2 Frequencies P-Values OR (95%CI)
1 20437634 20437764 rs7515774 20437634 A T 0.107 1.04E-06 1.10 (1.06–1.15) 2 PLA2G2D
1 67648596 67648596 rs76418789 67648596 G A 0.060 4.22E-07 0.88 (0.84–0.93) 1 IL23R (G149R)
1 112222702 112222702 rs534888 112222702 C T 0.467 7.16E-06 0.95 (0.92–0.97) 1 RAP1A
4 38324507 38373273 rs55843528 38361416 G A 0.245 1.89E-07 1.08 (1.05–1.11) 20
4 189893313 189893313 rs12647478 189893313 T C 0.391 7.58E-06 0.92 (0.88–0.95) 1
5 67691469 67691469 rs10068082 67691469 G A 0.037 1.72E-06 1.17 (1.10–1.26) 1 PIK3R1
5 158826792 158853941 rs56167332 158827769 C A 0.402 3.11E-07 1.07 (1.04–1.09) 21 IL12B
6 2957827 2966578 rs79536569 2957827 G A 0.017 3.50E-06 1.23 (1.13–1.35) 2 SERPINB6
6 32214010 32793981 rs184950714 32636728 G A 0.179 1.07E-17 1.16 (1.12–1.19) 452 (HLA)
7 12221801 12222116 rs200319458 12221801 T C 0.024 8.41E-06 1.19 (1.10–1.29) 2 TMEM106B
7 76948351 76948351 rs4727354 76948351 G T 0.051 3.31E-06 1.14 (1.08–1.20) 1 GSAP
8 70472493 70472493 rs117742432 70472493 G A 0.036 6.58E-06 0.86 (0.81–0.92) 1 SULF1
8 129224694 129245849 rs12678162 129224694 T C 0.431 3.08E-06 1.06 (1.03–1.08) 4 PVT1
9 73881874 73881874 rs151258497 73881874 C 0.331 4.57E-06 0.94 (0.92–0.97) 1 TRPM3
9 117480416 117697947 rs55951892 117575913 A C 0.490 1.76E-23 0.89 (0.860.91) 129 TNFSF15
10 64431973 64550071 rs224136 64470675 C T 0.275 1.18E-07 0.93 (0.90–0.95) 19 ZNF365
11 64908062 64926722 rs11227126 64908062 A T 0.067 1.71E-06 1.12 (1.07–1.18) 3 SYVN1
14 105695957 105695957 rs117952084 105695957 T C 0.021 9.73E-06 0.83 (0.76–0.90) 1 BRF1
15 27156539 27156539 rs781387485 27156539 ACACAA 0.095 3.36E-06 1.11 (1.06–1.16) 1 GABRA5
16 28513068 28531287 rs56354901 28523144 T C 0.134 2.44E-06 1.09 (1.05–1.13) 3 NPIPL1, IL27
19 30021446 30021446 rs117223925 30021446 G A 0.075 6.21E-06 0.90 (0.86–0.94) 1 VSTM2B
20 47804952 47804952 NA 47804952 CCCGGC 0.020 2.57E-06 1.21 (1.12–1.32) 1 STAU1
20 51548302 51548302 rs6126698 51548302 A T 0.484 8.31E-06 0.94 (0.91–0.97) 1 TSHZ2
21 33326781 33326781 rs2833577 33326781 G A 0.286 1.23E-06 1.07 (1.04–1.11) 1 HUNK
22 23054614 23054614 rs9623882 23054614 G A 0.081 1.61E-06 1.14 (1.08–1.20) 1 GGTLC2

*Positions are based on the Genome Reference Consortium human build 37 (GRCh37), **Number of SNPs with p values <1 × 10−5 Chr: Chromosome, OR: Odds ratio, CI: Confidential interval.