Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1150753 0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 2
rs1748033 0.925 0.120 1 17336167 missense variant T/C;G snv 0.63; 4.0E-06 2
rs1913517 0.925 0.120 10 48911009 intron variant A/G snv 0.54 2
rs2075876 0.925 0.120 21 44289270 non coding transcript exon variant G/A snv 0.19 2
rs3117103 0.925 0.120 6 32381780 intron variant A/T snv 9.6E-02 2
rs340630 0.925 0.120 4 87037243 intron variant G/A snv 0.42 2
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs509749
LY9
0.925 0.120 1 160823770 missense variant A/G snv 0.54 0.55 2
rs6935269 0.925 0.120 6 32292573 intron variant T/C snv 0.25 2
rs704853 0.925 0.120 1 167499627 intron variant G/T snv 0.15 2
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
rs7097397 0.925 0.120 10 48817351 missense variant G/A snv 0.38 0.31 2
rs7258015 0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs771131230 0.925 0.120 6 32581827 missense variant C/A;T snv 2
rs773389640 0.925 0.120 6 32581821 missense variant C/G;T snv 2
rs9275428 0.925 0.120 6 32703201 downstream gene variant A/C;G snv 2
rs9603612 0.925 0.120 13 39760715 intron variant C/G snv 0.30 2
rs1003878 0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs1077393 0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10840759 0.882 0.200 12 8138610 intron variant C/T snv 0.28 3
rs17581834 0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs2242665 0.882 0.160 6 31871532 missense variant C/T snv 0.60 0.60 3
rs2248932
BLK
0.882 0.160 8 11534141 intron variant A/G snv 0.60 3
rs2277798 0.925 0.120 21 42403997 missense variant A/G snv 0.55 0.60 3
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3