Table 2.

Genome-wide Significant Loci From GWASs of LTE

rsID	Chr	Positiona	A1	A2	A1 Frequency	z Score	p Value
rs6661135	1	150999414	C	T	0.93	−5.52	3.3 × 10−8
rs4665501	2	22546151	G	T	0.44	−5.77	7.7 × 10−9
rs4704792	5	155757946	A	T	0.26	5.75	9.2 × 10−9
rs1476535	7	114071035	C	T	0.44	−5.77	8.0 × 10−9
rs2933196	14	47285917	G	A	0.59	−5.51	3.6 × 10−8
rs770444611	19	46917381	INSb	T	0.59	5.66	1.5 × 10−8

A1, allele 1 (coded); A2, allele 2; Chr, chromosome; GWAS, genome-wide association study; LTE, lifetime trauma exposure; rsID, reference SNP ID number.

^aBase pair position on chromosome (hg19/GR37 Human Genome Build).

^bInsertion of TGAGGCCAGGAGTTC.