Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368287711 0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4
rs1475145065 0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs2027432 0.882 0.160 1 247415139 upstream gene variant A/G;T snv 3
rs2839693 0.882 0.120 10 44379119 intron variant T/A;C snv 3
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs5743867 0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs6958571 0.925 0.080 7 30446094 intron variant A/C;G snv 1.2E-05; 0.25; 5.3E-05 3
rs7119750 0.882 0.120 11 65655120 3 prime UTR variant C/G;T snv 3
rs773520745 0.882 0.120 19 18075817 missense variant C/G;T snv 2.0E-05; 4.0E-06 3
rs773829498 0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3
rs1153879 0.925 0.080 3 136392816 intron variant G/T snv 2
rs17602729 0.925 0.080 1 114693436 stop gained G/A;T snv 8.6E-02 2
rs1915087 0.925 0.080 3 122119944 3 prime UTR variant T/C snv 2
rs2332096 0.925 0.080 3 122102296 intron variant T/A;G snv 2
rs2715267 0.925 0.080 3 122052011 upstream gene variant G/A;T snv 2
rs41279766 0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs4755453 0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs595209 0.925 0.080 11 126292326 intron variant A/C;G snv 2
rs945177 1.000 0.080 13 27047848 intergenic variant G/A;T snv 1
rs1419560997 0.925 0.080 11 117993410 splice region variant G/A snv 8.0E-06 7.0E-06 2
rs41274221 0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs117983287 1.000 0.080 9 77405958 missense variant C/A snv 9.6E-03 8.3E-03 1