. Author manuscript; available in PMC: 2015 May 15.

Published in final edited form as: Am J Med Genet A. 2011 Sep 9;0(10):2453–2458. doi: 10.1002/ajmg.a.34225

Table I.

Results of genotyping analysis by SPSS version 13.0

Marker	Alleles	Patients homozygous for 35delG mutation (Chr=100)	Controls (Chr=100)	P value
D13S175(84785 bp telomeric)	1(107)	1 4	4	0.00000	☆
	2(109)	1	14
	3(111)	94	51
	4(113)	1	11
	5(115)	0	14
	6(117)	0	6
SNP4(34519 bp telomeric)	C	7	59	0.00000	☆
	T	93	41	0.00000	☆
SNP3(3588 bp telomeric)	C	100	24	0.00000	☆
	T	0	76	0.00000	☆
SNP2(3547 bp telomeric)	A	0	6	0.029	☆
	G	100	94	0.029	☆
SNP1(765 bp centromeric)	C	8	84	0.00000	☆
	T	92	16	0.00000	☆
D13S141(39262 bp centromeric)	1(116)	0	0	0.00000	☆
	2(118)	0	2
	3(120)	2	6
	4(122)	4	76
	5(124)	86	10
	6(126)	8	6
	7(130)	0	0
SNP5(62793 bp centromeric)	C	35	39	0.661
	T	65	61	0.661

^☆

shows the significant difference ( P value < 0.05) of the variable between cases and controls for those specific alleles.