Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35134728 0.882 0.120 1 11787277 3 prime UTR variant -/AGA delins 3
rs3737966 0.882 0.120 1 11787702 3 prime UTR variant C/T snv 0.55 3
rs4149009 0.882 0.120 12 21267537 3 prime UTR variant C/T snv 0.38 3
rs72481843 0.882 0.120 5 143300685 splice donor variant C/G snv 3
rs12434881 0.882 0.120 14 23119433 5 prime UTR variant G/A snv 0.36 3
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs201765376
MTR
0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05 12
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs7853758 0.851 0.120 9 84286011 synonymous variant G/A snv 0.15 0.19 5
rs569954362 0.851 0.160 21 45530871 synonymous variant G/A snv 4
rs57725551 0.882 0.120 21 45525868 synonymous variant G/T snv 5.3E-03 7.0E-03 3
rs6589664 0.882 0.120 11 118534089 synonymous variant G/A snv 0.30 0.27 3
rs12803915 0.882 0.120 11 65444508 non coding transcript exon variant G/A snv 0.16 0.17 3
rs62571442 0.882 0.120 9 134850278 non coding transcript exon variant G/A;C;T snv 0.58; 4.4E-03 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131