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. Author manuscript; available in PMC: 2011 Feb 1.
Published in final edited form as: Genet Epidemiol. 2010 Feb;34(2):171–187. doi: 10.1002/gepi.20449

Table 3.

Risk haplotypes and their corresponding frequencies in cases and controls for WTCCC HT and CAD data

Gene Chr Start SNP End SNP Haplotype Freq in cases Freq in controls Fisher’s exact test p-value
HT
ZFAT1 8 rs6988616 rs11778878 001000101111100101111101100100 0.001281 0.000173 4.21×10-2
001100100110110001000001101100 0.002049 0.000345 1.28×10-2
001110101011100001010111111010 0.011527 0 1.40×10-18
100100000101110011000001100100 0.004611 0.001553 4.94×10-3
111010101011100001010111111010 0.012295 0 8.95×10-20

CAD
CDKN2B 9 rs3217986 rs10965245 000000010000000010101111100000 0.011942 0.005956 1.27×10-3
100000010000000010101111100010 0.223780 0.189074 1.77×10-5
100000010000000010101111100011 0.015576 0.007658 1.55×10-4
101001101100111010101111100010 0.045691 0.037270 2.40×10-2
101111010000000010101111100010 0.011423 0.007488 2.45×10-2

EIF4H 7 rs150880 rs17146094 0100 0.011942 0.000511 1.13×10-15

HFE2 1 rs12091564 rs10218795 00 0.006490 0.000511 6.54×10-8

ZBTB43 9 rs10987465 rs7038622 01001101100101 0.006750 0.000851 5.15×10-7
01001111110001 0.003894 0.000511 1.86×10-4
01101111110001 0.003894 0.000340 4.90×10-5
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