Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1272388614 0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs1446306735 0.882 0.120 11 17395664 missense variant C/A;T snv 3
rs59852838 0.882 0.120 11 17453228 missense variant T/C snv 4.0E-05 4.9E-05 3
rs775776658 1.000 0.040 11 17474926 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.0E-05 1
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs534828104 0.925 0.080 3 186618566 missense variant A/G snv 2
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs3738435 0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs953686324 0.851 0.160 1 16044506 frameshift variant -/G delins 4.3E-06 5.6E-05 7
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs587777042 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 3
rs10139403 1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs4436578 0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs373269573 0.925 0.080 9 137711015 missense variant G/A snv 1.6E-04 9.1E-05 2
rs764437500 0.925 0.080 9 137716697 missense variant G/A snv 4.0E-06 2
rs8004664 0.925 0.080 14 89568628 intron variant G/A;C snv 3