Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs11103603 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 4
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs12442054 0.882 0.080 15 74165683 intron variant G/A snv 0.12 3
rs4758051 0.882 0.080 11 8217092 intergenic variant G/A snv 0.42 3
rs45511401
ABCC1
0.851 0.120 16 16079375 missense variant G/T snv 3.8E-02 3.6E-02 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
rs2271338
ADGRL3
0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs729147
ADH7
0.882 0.080 4 99412110 downstream gene variant G/A snv 0.78 3
rs773249771
ADRA1A
0.882 0.080 8 26864314 missense variant T/C snv 1.2E-05 3
rs1442511697
ADRA2B
0.882 0.080 2 96115494 missense variant T/C snv 7.0E-06 3
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs863225285
ALK
0.851 0.080 2 29209789 missense variant T/G snv 5
rs121909536
ANG ; RNASE4
0.827 0.120 14 20693686 missense variant A/T snv 1.2E-03 9.4E-04 5
rs121909539
ANG ; RNASE4
0.827 0.120 14 20693753 missense variant C/G snv 5
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72