Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs369410616 0.752 0.280 1 45329400 missense variant C/T snv 2.0E-05 2.8E-05 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
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
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
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
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48