Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs10931910
AOX1
0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs113017087
APC
1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 1
rs115658307
APC
1.000 0.040 5 112707537 5 prime UTR variant C/T snv 4.8E-03 1
rs138386816
APC
1.000 0.040 5 112707566 5 prime UTR variant C/T snv 7.2E-03 1
rs75612255
APC
1.000 0.040 5 112737543 intron variant T/C snv 1
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs7090445
ARID5B
0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 2
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31