Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003643 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 1
rs1003644 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 1
rs1005999 1.000 0.080 2 104907333 intron variant C/T snv 0.25 1
rs1008591 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 1
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs1011082
GSDMB
1.000 0.080 17 39912261 intron variant T/A;C snv 1
rs1015092
PLCB1
1.000 0.080 20 8769415 intron variant A/G;T snv 1
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10174098
ITGAV
0.882 0.200 2 186628015 intron variant G/A snv 0.62 3
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs1019212 1.000 0.080 19 46225962 upstream gene variant G/A snv 0.45 1
rs10234405
SDK1
1.000 0.080 7 4034827 intron variant A/G snv 0.33 1
rs10237319
SDK1
1.000 0.080 7 4033969 intron variant C/T snv 0.25 1
rs10237488
SDK1
1.000 0.080 7 4034710 intron variant T/G snv 0.33 1
rs10237838
SDK1
1.000 0.080 7 4034366 intron variant C/T snv 0.34 1
rs10265937
SDK1
1.000 0.080 7 4034017 intron variant G/A snv 0.32 1
rs10266101
SDK1
1.000 0.080 7 4034187 intron variant G/A;T snv 1
rs10278187
SDK1
1.000 0.080 7 4034741 intron variant C/G;T snv 1
rs1031458
GSDMB
1.000 0.080 17 39915920 intron variant G/A;T snv 1
rs10415976
ARID3A
1.000 0.080 19 941603 intron variant A/G snv 0.18 1
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs10445337
MAPT
0.925 0.120 17 45990034 missense variant T/C snv 0.15 0.15 3
rs10445371
MAPT
0.925 0.120 17 45988044 intron variant G/A snv 0.15 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10485860
SDK1
1.000 0.080 7 4050651 intron variant T/C snv 0.25 1