Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2378456
LPP
0.807 0.200 3 188885218 3 prime UTR variant C/G;T snv 6
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs3218977
IL1R2
0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs1064607
LPP
0.827 0.200 3 188877884 3 prime UTR variant G/C snv 0.46 5
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs12537
MTMR3 ; HORMAD2-AS1
0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs2412971
HORMAD2
0.882 0.320 22 30098382 intron variant G/A snv 0.55 5
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs8190315
BID
0.851 0.240 22 17743998 missense variant T/C snv 2.4E-02 3.6E-02 5
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs2071543
PSMB8-AS1 ; PSMB8
0.925 0.200 6 32843852 missense variant G/T snv 0.14 0.13 4
rs3796283
LPP
0.851 0.200 3 188885163 3 prime UTR variant A/G;T snv 4
rs5743557
TLR1
0.882 0.160 4 38805206 5 prime UTR variant G/A snv 0.14 4
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs1001703993
PPOX
0.882 0.120 1 161170696 missense variant G/A;T snv 8.0E-06 1.4E-05 3
rs11574637
ITGAX
0.882 0.200 16 31357553 missense variant T/C snv 0.21 3
rs1883414
HLA-DPB2
0.925 0.200 6 33118671 non coding transcript exon variant G/A snv 0.28 3
rs4849121
ACOXL
0.925 0.160 2 110842129 intron variant G/A snv 0.44 3
rs4984
LOC105374794 ; ADD2
0.925 0.160 2 70673271 synonymous variant G/A snv 0.12 0.15 3
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs1047763
C1GALT1
0.925 0.120 7 7243938 3 prime UTR variant G/A snv 0.22 2