Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs3807992
CAV1
0.925 0.080 7 116557191 intron variant G/A snv 0.28 5
rs10251201
UMAD1
0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs3757733
CAV1
1.000 0.040 7 116553675 intron variant T/A snv 0.26 4
rs6964823
IKZF1
0.925 0.040 7 50392398 intron variant G/A snv 0.45 3
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs1801280
NAT2
0.716 0.440 8 18400344 missense variant T/C snv 0.38 0.39 14
rs1470755915
RUNX1T1
0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs927698341
RUNX1T1
0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs778036161
RUNX1T1
0.776 0.080 8 92017363 missense variant T/C snv 8.0E-06 9
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs765669662
CA3-AS1 ; CA2
0.925 0.040 8 85465317 missense variant G/A;T snv 2.0E-05; 4.0E-06 2
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
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
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
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