Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1215029143 1.000 0.040 X 154558608 missense variant G/A;T snv 2
rs1227057051 1.000 0.040 21 43172266 missense variant G/A snv 8.2E-06 2
rs11260867 1.000 0.040 1 16115233 regulatory region variant C/G snv 0.13 1
rs1163215981 1.000 0.040 19 544073 start lost T/C snv 2.6E-05 1
rs1305547785 1.000 0.040 10 17229759 missense variant C/T snv 1
rs1314710813
MIP
1.000 0.040 12 56454277 stop gained G/A;C snv 4.0E-06 1
rs139609998 1.000 0.040 2 208145915 missense variant C/A;G snv 4.0E-06 1
rs143507827 1.000 0.040 3 186539542 missense variant T/C snv 5.6E-04 2.0E-04 1
rs147994059 1.000 0.040 17 29250258 missense variant G/A;C;T snv 1.1E-03; 4.0E-06 1
rs2289917 1.000 0.040 2 208146167 upstream gene variant G/A;C snv 0.33; 4.0E-06 1
rs2330991 1.000 0.040 22 25229562 missense variant C/T snv 2.8E-05 1
rs4613984 1.000 0.040 8 39919023 intron variant G/A;T snv 3.9E-02; 8.2E-06 1
rs531379398 1.000 0.040 13 20143205 synonymous variant C/T snv 8.0E-04 1.2E-04 1
rs532063800 1.000 0.040 1 9245310 missense variant G/A snv 4.0E-06 1
rs543287988 1.000 0.040 1 9245277 missense variant G/A snv 4.4E-05 7.0E-06 1
rs749808170 1.000 0.040 1 9245103 missense variant G/A snv 7.0E-06 1
rs751634469 1.000 0.040 20 33811532 missense variant C/A;T snv 4.2E-06; 8.5E-06 1
rs7543472 1.000 0.040 1 16113897 regulatory region variant C/A;G;T snv 1
rs758842039 1.000 0.040 22 25221431 start lost T/C snv 4.0E-06 1
rs762772949 1.000 0.040 2 208145956 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs763964114 1.000 0.040 19 547343 start lost T/A;C snv 3.6E-05; 1.3E-05 1
rs767347878 1.000 0.040 2 208163280 missense variant C/T snv 6.0E-05 1.4E-05 1
rs777547119
HGD
1.000 0.040 3 120675839 missense variant A/G snv 4.0E-06 1
rs778768887 1.000 0.040 2 208124472 start lost A/G snv 1.7E-05 1
rs782809283 1.000 0.040 11 111911693 missense variant C/T snv 1.8E-05 4.2E-05 1