Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041536 1.000 0.040 20 9907627 intergenic variant T/C snv 0.46 1
rs112961612 1.000 0.040 20 41872026 intergenic variant T/A snv 8.2E-02 1
rs113793030 1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02 1
rs115700680 1.000 0.040 1 171381070 intergenic variant T/G snv 1.9E-02 1
rs116065238 1.000 0.040 1 171482283 upstream gene variant A/G snv 4.3E-03 1
rs116237496 1.000 0.040 8 101033687 upstream gene variant T/C snv 4.0E-02 1
rs117070989 1.000 0.040 6 137490510 downstream gene variant C/A snv 8.3E-03 1
rs117129097 1.000 0.040 12 128054737 intron variant C/G;T snv 1.9E-03 1
rs117224174 1.000 0.040 6 114654261 intergenic variant G/A snv 2.2E-02 1
rs12230170 1.000 0.040 12 128762838 intergenic variant T/A;G snv 1
rs12435940 1.000 0.040 14 25552779 intergenic variant A/G snv 0.97 1
rs12468965 1.000 0.040 2 53528621 downstream gene variant G/A snv 1.8E-02 1
rs138901640 1.000 0.040 9 118031487 intron variant A/G snv 5.5E-03 1
rs139660738 1.000 0.040 12 94791412 intergenic variant T/C snv 6.3E-03 1
rs141480664 1.000 0.040 7 4469958 regulatory region variant G/A snv 1.0E-02 1
rs142609537 1.000 0.040 15 95675665 intron variant A/G snv 1.8E-02 1
rs146594485 1.000 0.040 20 3776090 downstream gene variant G/A snv 6.1E-03 1
rs149969998 1.000 0.040 17 13692262 intergenic variant G/C;T snv 1
rs150418526 1.000 0.040 17 38697587 upstream gene variant C/G;T snv 1
rs150616616 1.000 0.040 5 121366663 downstream gene variant C/G;T snv 1
rs150759334 1.000 0.040 4 60800528 downstream gene variant T/C snv 9.4E-03 1
rs150828104 1.000 0.040 12 116337891 regulatory region variant TTTTGTTTTG/-;TTTTG;TTTTGTTTTGTTTTG;TTTTGTTTTGTTTTGTTTTG delins 1
rs150934526 1.000 0.040 5 121330628 intron variant T/C snv 1.1E-02 1
rs183819925 1.000 0.040 4 175138126 intron variant G/T snv 9.7E-03 1
rs184148048 1.000 0.040 2 66212157 intergenic variant A/T snv 1.3E-02 1