Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4749812 1.000 0.080 10 8695601 intergenic variant G/C snv 0.42 1
rs6038071 1.000 0.080 20 584433 regulatory region variant C/T snv 0.14 1
rs66475048 1.000 0.080 11 63572600 downstream gene variant G/A snv 0.17 1
rs67052019 1.000 0.080 1 109822839 regulatory region variant TGTAGGGGCACAGAGAGA/-;TGTAGGGGCACAGAGAGATGTAGGGGCACAGAGAGA delins 1
rs7006896 1.000 0.080 8 129809948 regulatory region variant G/A snv 0.13 1
rs7136702 1.000 0.080 12 50486433 intergenic variant T/A;C snv 1
rs7547751 1.000 0.080 1 221892367 intron variant T/C snv 0.47 1
rs7667693 1.000 0.080 4 93944123 intergenic variant T/C snv 0.35 1
rs7898455 1.000 0.080 10 8696945 intergenic variant G/T snv 0.27 1
rs7988900 1.000 0.080 13 97826281 intergenic variant T/C snv 0.45 1
rs8180040 1.000 0.080 3 47347457 non coding transcript exon variant T/A snv 0.37 1
rs879872 1.000 0.080 11 256714 downstream gene variant C/T snv 4.1E-02 1
rs9588884 1.000 0.080 13 90145067 intergenic variant C/G snv 0.70 1
rs189206655
ABCA1
1.000 0.080 9 104809521 missense variant C/T snv 4.0E-06 1.4E-05 1
rs1202168
ABCB1
1.000 0.080 7 87566646 intron variant G/A snv 0.39 1
rs868755
ABCB1
1.000 0.080 7 87560614 intron variant T/G snv 0.68 1
rs3742106
ABCC4
1.000 0.080 13 95021537 3 prime UTR variant A/C snv 0.41 0.37 1
rs1357271377
ACACA
1.000 0.080 17 37161959 missense variant C/T snv 1.6E-05 1
rs754740225
ACAP1
1.000 0.080 17 7343420 missense variant G/A;T snv 3.6E-05; 4.0E-06 1
rs754494408
ACIN1
1.000 0.080 14 23061417 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs2304497
ACLY
1.000 0.080 17 41909521 missense variant T/C;G snv 4.0E-06; 0.10 0.11 1
rs753267653
ACSL4
1.000 0.080 X 109682851 missense variant G/A snv 2.7E-05 9.5E-06 1
rs782721280
ACTL9
1.000 0.080 19 8697708 missense variant C/T snv 1.6E-05 1
rs12997
ACVR1
1.000 0.080 2 157736845 3 prime UTR variant A/G snv 0.45 1
rs1178207005
ADAM19
1.000 0.080 5 157509314 missense variant C/T snv 7.0E-06 1