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. Author manuscript; available in PMC: 2016 May 1.
Published in final edited form as: Mol Psychiatry. 2014 Dec 2;20(11):1467–1478. doi: 10.1038/mp.2014.156

Table 3.

Significant Rare Variant Association Results Using Weighted Sum Statistic (WSS) in AA and EA Samples

Gene AA Sample EA Sample
SNPs Permuted p value SNPs Permuted p value
NRXN1 rs77665267 (p.T274P)
- (p.R206L)
- (p.Y367*)
- (p.S62*)
2.28×104 rs77665267 (p.T274P)
- (p.R206L)
2×106
CHRNA9 rs142807401 (p.A432T)
rs139982841 (p.A452V)
3.81×104 rs56210055 (p.A312T)
rs142807401 (p.A432T)
rs139982841 (p.A452V)
8×106
TAS2R38 rs139843932 (p.W135G)
rs114288846 (p.R274C)
0.5346 rs139843932 (p.W135G)
rs114288846 (p.R274C)
2×106
CHRNA2 - (p.S488*)
- (p.R121L)
1.31×104 N/A N/A
NTRK2 rs150692457 (p.L140F)
- (p.C623*)
4.25×104 N/A N/A
GABBR2 - (p.P742Q)
- (p.G671C)
1.58×104 N/A N/A
GRIN3A rs75981117 (p.N549S)
rs34755188 (p.R480H)
- (p.V389L)
- (p.V132L)
2.42×103 rs75981117 (p.N549S)
rs34755188 (p.R480H)
- (p.V389L)
- (p.V132L)
8×106
DNM1 rs61757224 (p.L16M)
- (p.S126*)
- (p.R228L)
- (p.Y231*)
3.53×104 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)
1×106
NRXN2 - (p.T1371P)
- (p.V53G)
- (p.E267G)
1.49×103 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*)
6×106
NRXN3 rs199840331 (p.Y234*)
- (p.G696*)
- (p.T99P)
2.17×104 - (p.G696*)
- (p.T99P)
1×106
CDH13 rs72807847 (p.N39S)
rs200591230 (p.V464I)
0.5231 rs72807847 (p.N39S)
rs200591230 (p.V464I)
3.5×105
ARRB2 - (p.T84P)
- (p.H281Q)
1.32×104 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.