Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs74501188
ADGRV1
1.000 0.080 5 90931162 5 prime UTR variant G/A snv 0.17 1
rs942190
TDP1 ; EFCAB11
1.000 0.080 14 89956320 intron variant T/C snv 0.37 2
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs117729306
STK33
1.000 0.080 11 8465623 non coding transcript exon variant T/C snv 7.3E-03 1
rs8049634
LOC654780 ; ADAD2
1.000 0.080 16 84192073 intron variant A/G snv 0.35 1
rs859
STARD5 ; IL16
0.807 0.200 15 81308981 3 prime UTR variant A/G snv 0.33 6
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs140013431
BMP6
1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs587781495
TP53
1.000 0.080 17 7676005 missense variant C/T snv 1
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26