Table 3: Allele frequencies in IBD cases and healthy controls.

SNP no. Position in NT_02257.18*IBD casesControls
N alleles includedN variant allelesAllele frequency in %N alleles includedN variant allelesAllele frequency in %

112332979G>T5660036410.27
212333068insC56610.1836400
312333070C>T5660036420.55
412333125C>G5666010.603645013.74
512333199T>G56610.1836400
612333213G>A5660036430.82
712361272C>T56210.1835800
812361422A>G5620035810.28
912363017A>G55410.1833400
1012374014G>T55410.1834800
1112374024A>T56410.1834800
1212374091C>A55410.1834800
1312374110C>T55410.1834800
1412374272A>T55410.1834810.29
1512374352C>T5540034810.29
1612387616G>A56210.1836000
1712398613C>T5460037010.27
2812415473G>A5460035010.29
1912415557C>T5466612.093504613.14
2012415581G>A5460035010.29
2112415647G>A54620.3735000
2212415669C>T5460035010.29

no.: number; N: absolute number; *DNA reference sequence signature in NCBI.