Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 15
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 9
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 6
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs6475526 1.000 0.080 9 21242162 upstream gene variant C/T snv 0.33 2
rs10964862 9 21151554 intergenic variant C/A;G snv 1
rs946486
ABL1
9 130770618 intron variant C/T snv 0.44 1
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 4
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs772893086
ADARB1
0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 9
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 6
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 9
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 4