Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049793
LOC105375567 ; AOC1
0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37 4
rs10499563
STEAP1B
0.807 0.120 7 22720869 intron variant T/C snv 0.21 7
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs10510607
CMC1
0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 3
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10870077
CARD9
0.827 0.120 9 136369439 intron variant C/G snv 0.38 5
rs10883365
LINC01475
0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 3
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10910092
LOC100996583
1.000 0.040 1 2570077 downstream gene variant A/G snv 0.52 1