Table 8.
Dominant([RR+RN] vs. NN) |
Heterozygotes(RR vs. NN) |
Recessive(RR vs. [RN+NN]) |
Homozygotes(RR vs. NN) |
||||||||||
SNP (Allele) | Gene | OR | 95% CI | AR | P | OR | AR | OR | 95% CI | AR | P | OR | AR |
rs6658788 (2) | .83 | .57–1.22 | −14.04 | .3909 | 1.09 | 2.69 | 1.01 | .68–1.5 | .21 | 1 | .88 | −5.92 | |
rs1538687 (2) | .68 | .49–.95 | −19.38 | .023 | .5 | −11.74 | .42 | .23–.78 | −6.52 | .0068 | .38 | −12.42 | |
rs1416962 (2) | .84 | .6–1.18 | −10.02 | .3418 | .89 | −2.57 | .82 | .49–1.38 | −2.31 | .5002 | .77 | −5.74 | |
rs946755 (2) | .8 | .57–1.13 | −12.52 | .232 | 1 | .04 | .9 | .53–1.52 | −1.24 | .7816 | .81 | −4.34 | |
rs6428352 (2) | … | … | … | … | … | … | … | … | … | … | … | … | |
rs800292 (1) | CFH | .43 |
.3–.62 | −30.01 |
<.0001 | .48 |
−23.85 |
.15 |
.05–.45 | −4.98 |
.0001 | .12 |
−8.19 |
rs1061170 (2) | CFH | 5.29 |
3.35–8.35 | 68.2 |
<.0001 | 2.66 | 28.55 | 4.57 |
2.48–8.42 | 30.06 |
<.0001 | 10.05 |
63.72 |
rs10922093 (1) | CFH | .59 | .39–.88 | −25.61 | .0111 | .63 | −19.65 | .5 | .24–1.04 | −4.98 | .0736 | .41 | −10.14 |
rs70620 (1) | CFH | .83 | .57–1.19 | −5.64 | .3366 | .85 | −4.29 | .67 | .27–1.68 | −1.3 | .4525 | .64 | −1.93 |
rs1853883 (2) | 2.67 |
1.78–4.01 | 54.41 |
<.0001 | 1.65 | 19.21 | 2.08 |
1.43–3.02 | 22.06 |
.0003 | 3.55 |
55.04 |
|
rs1360558 (1) | 1.16 | .82–1.65 | 9.12 | .414 | 1.1 | 5.39 | 1.25 | .8–1.96 | 3.94 | .3774 | 1.32 | 9.01 | |
rs955927 (2) | 1.13 | .79–1.6 | 7.5 | .5303 | 1.28 | 6.35 | 1.31 | .83–2.08 | 4.53 | .2588 | 1.36 | 9.38 | |
rs4350226 (2) | .51 | .32–.81 | −9.68 | .0038 | .27 | −4.76 | .16 | .01–1.74 | −.95 | .142 | .14 | −1.16 | |
rs4752266 (2) | GRK5 | .88 | .62–1.23 | −5.57 | .4325 | 3.27 | 10.68 | 2.81 | .98–8.04 | 3.89 | .0457 | 2.56 | 5.51 |
rs915394 (2) | GRK5 | 1.28 | .9–1.82 | 8.91 | .1543 | 1.35 | 2.73 | 1.56 | .58–4.14 | 1.53 | .3892 | 1.68 | 2.72 |
rs1268947 (2) | GRK5 | 1.05 | .7–1.57 | 1.06 | .841 | 1.24 | 1.82 | 1.27 | .35–4.55 | .45 | .7761 | 1.28 | .58 |
rs1537576 (2) | GRK5 | 1.59 | 1.11–2.29 | 27.95 | .0109 | .89 | −3.74 | 1.08 | .71–1.62 | 1.59 | .7579 | 1.47 | 15.14 |
rs2039488 (2) | .7 | .45–1.07 | −6.5 | .1067 | .23 | −11.98 | .19 | .04–.79 | −2.33 | .0242 | .18 | −2.85 | |
rs1467813 (1) | RGS10 | .96 | .69–1.35 | −1.84 | .8645 | 1.01 | .42 | .77 | .42–1.38 | −2.27 | .4265 | .77 | −3.76 |
rs927427 (1) | 1.09 | .74–1.62 | 6.57 | .6172 | .94 | −4.66 | 1.67 | 1.09–2.56 | 10.73 | .0201 | 1.6 | 19.91 | |
rs4146894 (1) | PLEKHA1 | 2.22 |
1.49–3.31 | 46.78 |
.0002 | 1.77 | 33.08 | 2.21 |
1.49–3.29 | 20.46 |
<.0001 | 3.31 |
49.88 |
rs12258692 (2) | PLEKHA1 | … | … | … | … | … | … | … | … | … | … | … | … |
rs4405249 (1) | PLEKHA1 | .62 | .33–1.15 | −12.96 | .1692 | .61 | −12.69 | .87 | .1–7.56 | −.23 | 1 | .77 | −.57 |
rs1045216 (2) | PLEKHA1 | .48 |
.32–.74 | −51.23 |
.0005 | .49 | −18.27 | .37 |
.21–.65 | −14.3 |
.0003 | .28 |
−35.68 |
rs1882907 (2) | .58 | .4–.84 | −16.73 | .0026 | .44 | −5.79 | .31 | .1–.97 | −2.37 | .0438 | .27 | −3.65 | |
rs10490923 (2) | LOC387715 | .53 | .31–.9 | −13.27 | .0239 | .34 | −9.01 | .22 | .04–1.09 | −2.51 | .0809 | .2 | −3.32 |
rs2736911 (2) | LOC387715 | .72 | .42–1.21 | −6.92 | .2552 | 1.47 | 1.99 | 1.1 | .13–9.53 | .1 | 1 | 1.03 | .04 |
rs10490924 (2) | LOC387715 | 5.03 |
3.2–7.91 | 57.11 |
<.0001 | 2.72 | 22.76 | 5.75 |
2.46–13.46 | 21.2 |
<.0001 | 10.57 |
42.71 |
rs11538141 (2) | PRSS11 | … | … | … | … | … | … | … | … | … | … | … | … |
rs760336 (2) | PRSS11 | .64 | .44–.93 | −35.37 | .013 | .8 | −6.95 | .69 | .46–1.03 | −7.95 | .0773 | .55 | −26.43 |
rs763720 (1) | PRSS11 | 1.69 | 1.2–2.38 | 21.24 | .0018 | 1.55 | 16.95 | 2.63 | 1.1–6.25 | 5.17 | .0277 | 3.16 | 10.14 |
rs1803403 (1) | PRSS11 | 2.98 | 1.25–7.06 | 10.51 | .0093 | 2.98 | 10.51 | … | … | … | … | … | … |
Note.— Type A–affected individuals are compared with controls. OR and AR values are underlined if corresponding P values are ⩽.001 and are in bold italics if P values are ⩽.05. Allele denotes the risk allele (minor allele in controls). RR = homozygotes for the risk allele; RN = heterozygotes for the risk allele; NN = homozygotes for the normal allele. Locally typed SNPs are in bold italics. Blank spaces separate the three chromosomal regions corresponding to SNPs in and around CFH, GRK5/RGS10, and PLEKHA1/LOC687715/PRSS11.