Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10155912 1.000 0.040 7 140058921 intron variant A/C snv 0.48 1
rs10200159 1.000 0.040 2 55617974 non coding transcript exon variant T/C snv 0.14 1
rs10249788 0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs10250629 1.000 0.040 7 50151757 intron variant T/C snv 0.41 1
rs1031034 1.000 0.040 4 101302229 intron variant C/A snv 0.29 1
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1043101 1.000 0.040 11 35253282 3 prime UTR variant A/G;T snv 1
rs10431924 0.882 0.120 16 68805399 intron variant T/C snv 0.45 3
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs10503019 0.925 0.040 18 57787145 intron variant G/A snv 0.17 2
rs10768122 1.000 0.040 11 35259305 3 prime UTR variant A/G snv 0.33 1
rs10774624 0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs1079541 1.000 0.040 6 30438979 intergenic variant C/A snv 0.17 1
rs10876864 0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 5
rs10986311 1.000 0.040 9 124309214 intron variant T/C snv 0.34 1
rs11021232 1.000 0.040 11 95587644 intron variant T/C snv 0.14 1
rs11079035 1.000 0.040 17 42136994 intron variant G/A snv 0.29 3
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs1129038 0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 8
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1135216 0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 6
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70