Table 3.
Gene | AA Sample | EA Sample | ||
---|---|---|---|---|
SNPs | Permuted p value | SNPs | Permuted p value | |
NRXN1 |
rs77665267 (p.T274P) - (p.R206L) - (p.Y367*) - (p.S62*) |
2.28×10−4 |
rs77665267 (p.T274P) - (p.R206L) |
2×10−6 |
CHRNA9 |
rs142807401 (p.A432T) rs139982841 (p.A452V) |
3.81×10−4 | rs56210055 (p.A312T) rs142807401 (p.A432T) rs139982841 (p.A452V) |
8×10−6 |
TAS2R38 |
rs139843932 (p.W135G) rs114288846 (p.R274C) |
0.5346 |
rs139843932 (p.W135G) rs114288846 (p.R274C) |
2×10−6† |
CHRNA2 | - (p.S488*) - (p.R121L) |
1.31×10−4 | N/A | N/A |
NTRK2 | rs150692457 (p.L140F) - (p.C623*) |
4.25×10−4 | N/A | N/A |
GABBR2 | - (p.P742Q) - (p.G671C) |
1.58×10−4 | N/A | N/A |
GRIN3A |
rs75981117 (p.N549S) rs34755188 (p.R480H) - (p.V389L) - (p.V132L) |
2.42×10−3 |
rs75981117 (p.N549S) rs34755188 (p.R480H) - (p.V389L) - (p.V132L) |
8×10−6 |
DNM1 | rs61757224 (p.L16M) - (p.S126*) - (p.R228L) - (p.Y231*) |
3.53×10−4 | N/A | N/A |
DBH |
rs182974707 (p.I340T) rs75215331 (p.A362V) - (p.Y389*) - (p.T395P) rs41316996 (p.G482R) rs6271 (p.R549C) |
0.2427 |
rs182974707 (p.I340T) rs75215331 (p.A362V) rs41316996 (p.G482R) |
1×10−6 |
NRXN2 | - (p.T1371P) - (p.V53G) - (p.E267G) |
1.49×10−3 | N/A | N/A |
ANKK1/DRD2 |
rs35877321 (p.R122H) rs56047699 (p.R237*) - (p.S313*) rs186633697 (p.P351S) rs56299709 (p.E376K) rs184645039 (p.E458G) rs113005509 (p.E587*) rs202222056 (p.Q657*) - (p.R734C) - (p.E181*) |
0.8114 | rs111789052 (p.C52W) rs35877321 (p.R122H) rs115800217 (p.R185Q) rs56047699 (p.R237*) - (p.S313*) rs56299709 (p.E376K) rs78229381 (p.R445C) rs184645039 (p.E458G) rs113005509 (p.E587*) - (p.R734C) - (p.E181*) |
6×10−6 |
NRXN3 | rs199840331 (p.Y234*) - (p.G696*) - (p.T99P) |
2.17×10−4 |
- (p.G696*) - (p.T99P) |
1×10−6† |
CDH13 |
rs72807847 (p.N39S) rs200591230 (p.V464I) |
0.5231 |
rs72807847 (p.N39S) rs200591230 (p.V464I) |
3.5×10−5† |
ARRB2 | - (p.T84P) - (p.H281Q) |
1.32×10−4 | N/A | N/A |
P value based on 108 permutations.
Notes:
1) Permuted p value = value based on 106 permutations; - = not reported in dbSNP database by 2/17/2014; N/A = not applicable; i.e., without two rare nonsynonymous variants in gene or region.
2) SNPs included in both AA and EA rare variant analysis are underlined.
3) Significant association p values after correction for multiple testing(p< 2.63×10−3 for AA sample and p< 4.55×10−3 for EA sample) are given in bold. See “Materials and Methods” for details.