Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 8
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 7
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs16903574
OTULINL
0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 6
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs11096955
TLR10
0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 5
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3