Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs397507545 0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20
rs872071 0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs3138053 0.790 0.280 14 35405648 upstream gene variant T/C snv 0.26 10
rs182123615 0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 7
rs9268403 0.807 0.240 6 32373696 intron variant T/C snv 0.24 6
rs121964877 0.851 0.160 16 68822081 stop gained C/G;T snv 5
rs56302315
KDR
0.827 0.160 4 55089802 missense variant C/T snv 5.3E-04 4.1E-04 5