Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs752967378 0.882 0.160 3 12618580 missense variant G/A;C snv 4.0E-06 3
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs3749474 0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144