Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28665122
SELENOS
0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 6
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2618431
FAM167A
0.925 0.120 8 11466955 intron variant A/G snv 0.87 2
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs4840568
BLK
0.882 0.160 8 11493510 intron variant G/A snv 0.32 4
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs7629750
TMEM39A
0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5
rs2069550
TG
0.925 0.120 8 132888141 synonymous variant T/C snv 0.58 0.60 2
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs2076740
TG
0.827 0.160 8 132971813 missense variant C/T snv 0.31 0.37 5
rs661561
TNFAIP3
0.882 0.200 6 137876194 intron variant A/C snv 0.62 0.50 3
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs7514229
TNFSF4
1.000 1 173185165 3 prime UTR variant G/T snv 0.43 1
rs745826707
RBM45
0.851 0.200 2 178112712 missense variant G/A;T snv 8.0E-06; 4.0E-06 5
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44