Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750072 1.000 0.080 17 45983493 missense variant A/G snv 4.0E-02 3.8E-02 3
rs63751165 0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs1426868527 1 20633841 missense variant G/A;T snv 3
rs1555727942 0.925 0.160 19 15180807 missense variant G/A snv 3
rs752078407 1.000 0.080 20 3910806 missense variant A/T snv 6.4E-05 3.5E-05 3
rs137852538 0.925 0.080 X 78117385 missense variant A/T snv 3
rs74315360 0.925 0.040 1 20638104 missense variant C/A snv 3
rs74315356 0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs369634041 6 162262647 missense variant C/A;T snv 4.0E-06; 2.0E-05 3
rs781442277 1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs1290141855 1.000 0.040 16 55698539 missense variant T/C snv 4.0E-06 7.0E-06 3
rs80338892
TH
1.000 0.040 11 2167905 missense variant C/T snv 1.1E-04 1.4E-04 3
rs886039227 0.925 0.200 2 74378123 missense variant A/C snv 4
rs121918304 0.925 0.080 22 32498453 stop gained C/A;T snv 4.0E-06; 4.0E-06 4
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs2942168 0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 4
rs71653619 1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs41549716 0.882 0.200 15 89321842 missense variant T/C snv 6.6E-03 7.0E-03 4
rs368134308 0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs761807915 0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs63750444 0.882 0.080 14 73192745 missense variant G/A snv 4
rs3135500 0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5
rs45539432 0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs121908683 0.925 0.080 22 38115667 missense variant G/A snv 9.0E-06 2.1E-05 5
rs74315414 0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5