Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs6682925
C1orf141 ; IL23R
0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs12343867
INSL6 ; JAK2
0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs11574311
WRN
0.776 0.160 8 31119144 intron variant T/C snv 0.16 8
rs7309123
LOC105369655 ; CLEC7A
0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs3901533
CLEC7A ; LOC105369655
0.827 0.280 12 10124484 intron variant A/C snv 0.66 6
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs3812036
SLC34A1
0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5