Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs623590
HRH4
0.925 0.080 18 24463389 intron variant T/A;C snv 0.88 2
rs2241745
IRS2
0.882 0.120 13 109770184 intron variant C/T snv 0.88 4
rs2588814
RAD51B
1.000 0.080 14 68177081 intron variant G/A snv 0.87 1
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs2038979
RAD51B
1.000 0.080 14 68183059 intron variant G/A snv 0.87 1
rs2588819
LOC105370546 ; RAD51B
1.000 0.080 14 68161963 intron variant T/C snv 0.87 1
rs2745559 0.925 0.080 1 186682870 upstream gene variant A/C;T snv 0.87 2
rs11096688 1.000 0.080 2 20885650 intergenic variant T/C snv 0.86 1
rs518162
PGR ; PGR-AS1
0.925 0.080 11 101129770 5 prime UTR variant A/G snv 0.86 2
rs6472903
CASC9
0.925 0.080 8 75318066 intron variant G/T snv 0.86 2
rs1410669 1.000 0.080 6 71740732 intergenic variant G/A snv 0.85 1
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 7
rs2588808
RAD51B
1.000 0.080 14 68193464 intron variant A/G snv 0.84 1
rs7558615
ERBB4
0.925 0.080 2 212081424 intron variant T/C snv 0.84 4
rs888663 0.925 0.080 19 18374112 upstream gene variant G/T snv 0.84 2
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs2494744
AKT1
0.925 0.080 14 104789477 intron variant A/G snv 0.83 2
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs2243905
LOC105370546 ; RAD51B
1.000 0.080 14 68166696 intron variant G/A snv 0.83 1
rs4848599 1.000 0.080 2 120481784 intergenic variant T/C snv 0.82 1
rs2726492
TET2-AS1 ; TET2
1.000 0.080 4 105274384 intron variant T/C snv 0.82 1
rs1059476
AURKB
0.925 0.080 17 8205013 missense variant A/G snv 0.83 0.81 2