Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs157077 1.000 0.080 10 104278136 intron variant T/C snv 0.45 0.53 3
rs200397144 1.000 5 251427 missense variant C/G;T snv 2.4E-05; 4.0E-06 3
rs2231292 1.000 0.040 15 52112665 missense variant A/C snv 0.41 0.48 3
rs375878504 1.000 0.080 11 532741 synonymous variant G/A;C snv 8.1E-06 7.0E-06 3
rs397516434 1.000 0.120 17 7670669 missense variant G/A;T snv 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs560890523 1.000 0.080 12 25205729 3 prime UTR variant TT/-;T delins 3
rs573154688 1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05 3
rs587782359 1.000 0.080 16 68812244 missense variant C/G;T snv 2.8E-05 3
rs63750790 1.000 0.160 2 47476425 missense variant G/A snv 3.2E-05 7.0E-06 3
rs660652 1.000 0.080 15 78595490 3 prime UTR variant A/G;T snv 3
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs751477326 1.000 0.080 17 7675082 missense variant G/A;C snv 4.0E-06 3
rs7521584 1.000 0.040 1 1168578 upstream gene variant T/A;G snv 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs80291436
VCX
1.000 0.080 X 7843706 missense variant T/A;C;G snv 4.9E-05; 0.19 3
rs876659253 1.000 17 43094296 frameshift variant ACAT/TG delins 3
rs886039463 1.000 0.080 12 112489096 missense variant C/A snv 3
rs971586985 1.000 0.160 1 193212458 missense variant G/A;T snv 4.0E-06 2.1E-05 3
rs9862 1.000 0.080 22 32857293 missense variant T/A;C snv 4.0E-06; 0.55 3
rs1010898370 1.000 2 208243469 missense variant T/C;G snv 8.0E-06 2
rs1014509103 1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05 2
rs1040264140 1.000 0.080 15 90881744 missense variant A/G snv 2
rs1047325 1.000 0.040 1 153561551 missense variant C/T snv 7.1E-02 0.16 2
rs104894310 1.000 0.040 11 112086921 stop gained G/A snv 2