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. Author manuscript; available in PMC: 2010 Apr 5.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):341–351. doi: 10.1002/ajmg.b.30816

Table 2.

Frequency of Variant Allele among ethnic groups for the resequencing subjects

Frequency of Variant Allele
Location Nucleotide Sequence
Change
African-
America
n
Caucasia
n
Han
Chinese
America
n
Mexican
America
n
5′FR -3745 T-->A 0.042 0.000 0.000 0.000
5′FR -3636 T-->C 0.110 0.000 0.000 0.000
5′FR -3631 G-->A 0.025 0.050 0.000 0.042
5′FR -2063 to -
1714
44 bp
deletion
0.377 0.404 0.712 0.644
5′FR -1090 A-->T 0.017 0.000 0.000 0.000
5′FR -1089 A-->T 0.373 0.067 0.060 0.050
5′FR -859 A-->C 0.083 0.000 0.000 0.000
5′FR -482 T-->C 0.083 0.075 0.150 0.058
5′FR -469 C-->T 0.000 0.042 0.000 0.000
Intron 1b -45 C-->A 0.475 0.800 0.900 0.868
Intron 1b -25 G-->A 0.000 0.025 0.000 0.000
5′UTR -185 A-->C 0.325 0.200 0.108 0.125
5′UTR -149 C-->A 0.108 0.000 0.000 0.025
Intron 1a 28 G-->A 0.000 0.033 0.000 0.000
Exon 2 303 T-->C 0.025 0.008 0.000 0.000
Intron 2 VNTR -9 0.000 0.018 0.000 0.000
VNTR -10 0.319 0.436 0.070 0.276
VNTR -12 0.681 0.545 0.930 0.724
Intron 4 -100 G-->A 0.108 0.000 0.000 0.008
Intron 7 83 C-->T 0.017 0.025 0.000 0.008
Exon 8 1149 C-->T 0.000 0.000 0.000 0.033
Intron 11 -131 C-->T 0.066 0.000 0.000 0.000