Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15