Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 8
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42 4
rs189897
ITGA9
1.000 0.120 3 37477054 intron variant T/A snv 0.13 2
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 2
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 2
rs162171
CEP128
14 80794033 intron variant A/C snv 0.64 1
rs17111237
CEP128
14 80939997 intron variant A/G snv 0.15 1
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 4
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 2
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 2
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26