Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117834366 0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 2
rs10491487 1.000 0.120 5 81027549 intron variant T/G snv 8.2E-02 1
rs12007229 1.000 0.120 X 67528513 upstream gene variant C/A snv 0.11 1
rs2497931 1.000 0.120 X 67436434 intergenic variant A/C;T snv 1
rs26906 1.000 0.120 5 81069068 intron variant T/C snv 0.86 1
rs290227
SYK
1.000 0.120 9 90874382 intron variant G/A snv 0.30 1
rs4485213 1.000 0.120 13 105256524 intergenic variant C/T snv 0.19 1
rs951660 1.000 0.120 3 111919285 intron variant A/C snv 0.86 1
rs3813034 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs769665945 0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 3
rs140701 0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs944050 0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 5
rs17501010 0.827 0.320 3 190308865 intron variant G/T snv 0.15 5
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs893051 0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134