Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs736707 0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs756472 0.925 0.040 16 14185624 intron variant G/A snv 0.24 2
rs7608798 0.925 0.040 2 162033707 intron variant G/A snv 0.35 2
rs7794745 0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs779867 0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs112795301 0.776 0.160 3 70972634 stop gained G/A snv 13
rs10951154 0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917893 0.807 0.160 X 71167508 missense variant C/T snv 10
rs1460808228 0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800561 0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs201551401 0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs2736654 0.882 0.120 6 38682852 missense variant T/A;G snv 4
rs28364997 0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs35424709 0.925 0.040 3 193454190 missense variant T/A snv 8.6E-02 7.8E-02 2
rs35678 0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47 2
rs362691 0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 3
rs370911031 0.925 0.040 9 130219801 missense variant G/A snv 1.5E-04 8.4E-05 2
rs3735653
EN2
0.925 0.040 7 155458738 missense variant C/G;T snv 0.54 2
rs3747333 0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21