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. Author manuscript; available in PMC: 2018 Oct 25.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2017 Apr 25;174(5):557–567. doi: 10.1002/ajmg.b.32540

Table II.

Summary statistics for the gene-based test of rare variants in the UCSF Family Alcoholism study

CHR BEGIN END GENE Variant No. P
1 231762651 232172555 DISC1 16 1.72E-01
1 154245225 154247908 HAX1 3 2.80E-02
1 154542792 154548331 CHRNB2 6 1.00E+00
3 54156747 55107846 CACNA2D3 14 7.71E-01
6 29571342 29600126 GABBR1 2 1.90E-01
8 12943795 13357567 DLC1 29 7.29E-01
8 77895667 77913120 PEX2 9 3.35E-01
9 18533279 18906866 ADAMTSL1 20 1.00E+00
9 3828355 4286526 GLIS3 20 3.00E-01
14 45369682 45374747 C14ORF28 3 5.13E-01
14 45403373 45414662 KLHL28 6 1.00E+00
15 78873272 78885473 CHRNA5 3 5.33E-01
15 78885473 78911261 CHRNA3 5 5.66E-01
15 78917316 79012516 CHRNB4 10 3.96E-01
20 61978149 62005888 CHRNA4 12 6.71E-01

CHR: chromosome; BEGIN: the start position of gene; END; the end position of gene; Variant No.: the valid available rare nonsynonymous variants. P: the EMMAX SKAT association P-value.