Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs772572695 1.000 0.040 1 151406427 missense variant C/A;T snv 2.5E-05 1
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 1
rs756691187 1.000 0.040 1 151404993 missense variant C/G snv 8.0E-06 7.0E-06 1
rs782521991 0.925 0.040 X 154400848 missense variant C/G snv 3.5E-05 2.8E-05 1
rs796053483 1.000 0.040 16 2060775 missense variant C/G snv 7.0E-06 1
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs870142 0.851 0.120 4 4646320 intron variant C/G;T snv 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1452075 1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs797045050 0.807 0.120 2 240797715 missense variant C/T snv 4
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs121917893 0.807 0.160 X 71167508 missense variant C/T snv 2
rs1553518509 1.000 0.040 2 148468916 stop gained C/T snv 2
rs2230365 0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13 2
rs1452048149 1.000 0.040 1 151404828 missense variant C/T snv 4.0E-06 1
rs1557870645 1.000 0.040 1 151407271 missense variant C/T snv 1
rs375712202 1.000 0.040 11 124923339 splice donor variant C/T snv 9.6E-05 1.4E-05 1
rs4534 0.925 0.240 8 142879686 missense variant C/T snv 8.4E-02 4.1E-02 1
rs61753971 0.925 0.120 X 154030546 missense variant C/T snv 1.3E-04 1.1E-04 1
rs6824295 0.851 0.120 4 4612553 intron variant C/T snv 0.20 1
rs753214391 1.000 0.040 1 151406444 missense variant C/T snv 1.0E-05 2.1E-05 1
rs754532606 1.000 0.040 1 151423526 missense variant C/T snv 8.0E-06 2.1E-05 1
rs760059077 1.000 0.040 1 151405919 missense variant C/T snv 2.4E-05 2.1E-05 1
rs763820362 1.000 0.040 1 151424045 missense variant C/T snv 2.4E-05 1
rs769236847 0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 1