Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2240064
CCHCR1
1.000 0.120 6 31146796 intron variant G/A;T snv 1
rs2242660
PRRC2A
0.925 0.160 6 31629976 intron variant G/A snv 0.46 2
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs2516513
MICB-DT
0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 5
rs2523710
MICB-DT
1.000 0.120 6 31483132 intron variant G/A snv 0.14 1
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 5
rs2855430
COL11A2
1.000 0.120 6 33173503 missense variant G/A snv 0.12 9.9E-02 1
rs3093998 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 1