Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome

Table 3 Results of haplotype analysis in the AS case–control study

Number of SNPs	Haplotype combination	Chromosomal position	P value	FWER corrected P value
2	rs2268493-rs2254298	8800840-8802228	0.00086	0.00468
3	rs2268490-rs2268493-rs2254298	8797085-8802228	0.000365	0.0018
3	rs2268493-rs2254298-rs53576	8800840-8804371	0.00208	0.01268
4	rs237885-rs2268490-rs2268493-rs2254298	8795543-8802228	0.0012	0.00712
4	rs2268490- rs2268493-rs2254298-rs53576	8797085-8804371	0.00132	0.0079

Haplotypes with significant P values after permutation correction are reported. AS, Asperger Syndrome; FWER, family-wise error rates; SNPs, single nucleotide polymorphisms.

ISSN: 2040-2392