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. Author manuscript; available in PMC: 2016 Oct 11.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2014 Jul 1;165B(6):521–530. doi: 10.1002/ajmg.b.32255

Table 2.

Regions with p<0.01 from homozygous haplotype sharing analysis in overlapping ROH regions identified by PLINK

Chr Start End Number of
SNPs		 MQLS P-value
for homozygous
haplotype		 Gene(s) or
closest gene(s)
10 86,900,441 87,102,314 37 7.8·10−5 GRID1
6 28,512,017 29,225,795 38 8.7·10−3 ZNF311, TRIM27,
SCAND3, LOC401242,
OR2W1, OR2J3, OR2B3,
LOC100129636, OR2J2
12 59,917,023 61,612,551 114 9.6·10−3 SLC16A7
2 100,246,927 101,139,604 108 9.9·10−3 AFF3, BC105019,
LONRF2, CHST10, NMS