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. 2017 Aug 9;7:7630. doi: 10.1038/s41598-017-06737-4

Table 4.

SNPs which showed association with super-shedding phenomena.

Gene Variant.ID Location Alleles Freq_NS* Freq_SS** Consequence p-value
APOA1 rs384985356 15:27932563 A/C A, 50% A, 100% Synonymous variant 0.033
BATF2 rs42191303 29:43828428 C/T C, 100% C, 20% Intron variant 0.001
BLNK rs42088770 26:17382354 A/T A, 100% A, 50% Intron variant 0.033
BLNK rs110491800 26:17395942 A/G A, 50% A, 100% Intron variant 0.033
BLNK rs110241837 26:17398172 G/T G, 0% G, 70% Intron variant 0.003
BLNK rs109825977 26:17398543 A/G A, 0% A, 60% Intron variant 0.011
BLNK rs209836657 26:17398630 G/C G, 0% G, 70% Intron variant 0.003
BLNK rs42088798 26:17399306 G/C G, 0% G, 70% Intron variant 0.003
BLNK rs385916156 26:17399758 T/A T, 0% T, 60% Intron variant 0.011
BLNK rs211039227 26:17401401 T/A T, 0% T, 60% Intron variant 0.011
BLNK rs42088814 26:17401969 A/G A, 100% A, 40% Intron variant 0.011
BLNK rs42088815 26:17402059 T/C T, 100% T, 50% Intron variant 0.033
BLNK rs42084078 26:17419883 A/G A, 0% A, 50% Missense variant 0.033
BLNK rs135453434 26:17427529 C/T C, 100% C, 50% Intron variant 0.033
BLNK rs42084065 26:17428014 T/C T, 100% T, 50% Intron variant 0.033
BLNK rs132877528 26:17431964 C/T C, 0% C, 50% Intron variant 0.033
BLNK rs134560601 26:17432163 A/G A, 0% A, 60% Intron variant 0.011
IL18R1 rs109078612 11:7153863 T/C T, 0% T, 60% Intron variant 0.011
IL18R1 rs109700098 11:7169952 T/C T, 0% T, 60% Intron variant 0.011
IL18R1 rs109755291 11:7179544 C/T C, 0% C, 60% Missense variant 0.011
ITK rs109137099 7:70923893 T/C T, 80% T, 20% Intron variant 0.023
THEMIS rs135858596 9:66782892 C/A C, 30% C, 90% Intron variant 0.020
THEMIS rs207702093 9:66756813 C/T C, 100% C, 50% Intron variant 0.033
EBF1 rs207972417 7:72475725 C/T C, 100% C, 40% Intron variant 0.011
EBF1 rs207622846 7:72477936 T/C T, 100% T, 50% Intron variant 0.033
EBF1 rs209147903 7:72478125 G/A G, 100% G, 40% Intron variant 0.011
EBF1 rs211282271 7:72478236 T/C T, 100% T, 50% Intron variant 0.033
EBF1 rs384133035 7:72481066 A/G A, 100% A, 50% Intron variant 0.033
EBF1 rs41656033 7:72582112 G/C G, 100% G, 30% Intron variant 0.003
EBF1 rs132998336 7:72588676 G/A G, 90% G, 30% Intron variant 0.020
EBF1 rs135578882 7:72616057 C/T C, 100% C, 40% Intron variant 0.011
EBF1 rs43524161 7:72701165 C/G C, 50% C, 0% Intron variant 0.033
EBF1 rs29027619 7:72710782 G/C G, 70% G, 10% Intron variant 0.020

*Allele frequency in non-shedders, total frequency of two alleles are 100%.

**Allele frequency in super-shedders, total frequency of two alleles are 100%.