Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs28935197
GLA ; RPL36A-HNRNPH2
0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs2294021
CCDC22
0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs281874762
COL4A5
0.882 0.160 X 108578114 stop gained G/A;T snv 5.5E-06 3
rs281874682
COL4A5
0.925 0.080 X 108598805 missense variant C/A;T snv 5.5E-06 2
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs73885319
APOL1
0.851 0.120 22 36265860 missense variant A/G snv 1.6E-02 6.6E-02 6
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs60910145
APOL1
0.851 0.120 22 36265988 missense variant T/G snv 1.6E-02 6.6E-02 5
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs2032487
MYH9
0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs11089781
APOL3
0.925 0.080 22 36160720 stop gained G/A snv 1.6E-02 6.5E-02 2
rs117935223
PRODH
1.000 0.080 22 18923820 non coding transcript exon variant C/A snv 2
rs2413396
MYH9
0.925 0.080 22 36312039 intron variant C/G;T snv 0.88 2
rs138572244
C22orf31
1.000 0.080 22 29065297 upstream gene variant G/A snv 6.6E-03 1
rs4821469 1.000 0.080 22 36220399 intergenic variant T/C snv 0.21 1
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs2838302
SIK1
0.925 0.080 21 43419273 intron variant A/G snv 1.0E-01 2
rs187652497 1.000 0.080 21 41628325 regulatory region variant T/C snv 7.4E-03 1
rs2837554
DSCAM
1.000 0.080 21 40295451 intron variant A/G snv 0.78 1