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. Author manuscript; available in PMC: 2010 Feb 17.
Published in final edited form as: Eur J Neurol. 2007 Dec 18;15(2):134. doi: 10.1111/j.1468-1331.2007.02012.x

Table 2.

UCHL1 S18Y genotype and allele frequencies for total sample and sample stratified by age at onset and age at blood draw

Stratification by AAOa
Stratification by ABD
Total sample
Early-onset
Late-onset
Younger
Older
PD Controls PDb Controlsc PDd Controlse PDf Controlsf PDg Controlsg
Genotype countsh, n (proportion)
 CC 1191 (0.68) 1324 (0.66) 310 (0.70) 247 (0.69) 879 (0.67) 1077 (0.65) 507 (0.69) 579 (0.65) 684 (0.67) 745 (0.66)
 CA 509 (0.29) 621 (0.31) 121 (0.27) 102 (0.28) 387 (0.29) 519 (0.31) 201 (0.28) 278 (0.31) 308 (0.30) 343 (0.30)
 AA 57 (0.03) 71 (0.03) 12 (0.03) 11 (0.03) 45 (0.03) 60 (0.04) 22 (0.03) 33 (0.04) 35 (0.03) 38 (0.03)
Allele frequency, (A allele) 0.18 0.19 0.16 0.17 0.18 0.19 0.17 0.19 0.18 0.19
Test for HWEi (P) 0.74 0.94 0.96 0.85 0.78 0.87 0.69 0.96 0.96 0.92

AAO, age at onset; ABD, age at blood draw; HWE, Hardy–Weinberg equilibrium.

a

AAO information is missing for three individuals;

b

AAO ≤ 50 years;

c

ABD ≤ 50 years;

d

AAO > 50 years;

e

ABD > 50 years;

f

ABD ≤ 67 years;

g

ABD > 67 years;

h

at UCHL1 S18Y the S variant is encoded by the C allele and the Y variant is encoded by the A allele;

i

Test of HWE, P-value from an exact test.