Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs528557
ADAM33
0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 6
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs3918396
ADAM33
0.851 0.120 20 3671118 missense variant C/T snv 5.1E-05; 7.6E-02 6.7E-02 5
rs2280090
ADAM33
0.882 0.120 20 3669558 missense variant G/A snv 0.13 0.14 4
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 3
rs201256810
IL18R1 ; IL1RL1
0.925 0.080 2 102348073 missense variant C/T snv 2
rs345983
MGST2 ; MAML3
1.000 0.040 4 139717809 3 prime UTR variant C/T snv 0.62 1
rs1344110
PTTG1IP
1.000 0.040 21 44852737 intron variant T/C snv 0.18 1