Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473573 0.925 0.120 3 38604007 missense variant A/C snv 1.6E-05 7.0E-06 2
rs199473120 1.000 0.120 3 38604014 missense variant A/C snv 2.4E-05 1
rs199473092 0.925 0.080 3 38608175 missense variant A/C snv 1
rs199473053 1.000 0.080 3 38630422 missense variant A/C snv 1
rs199473176 1.000 0.080 3 38585728 missense variant A/C snv 1
rs199473050 1.000 0.080 3 38633098 missense variant A/C snv 4.4E-05 1.4E-05 1
rs199473232 1.000 0.080 3 38560340 missense variant A/C snv 1
rs199473221 1.000 0.080 3 38560424 missense variant A/C snv 1
rs199473274 1.000 0.080 3 38554380 missense variant A/C snv 1
rs199473236 1.000 0.080 3 38560313 missense variant A/C snv 1
rs199473566 1.000 0.080 3 38606689 missense variant A/C snv 1
rs199473256 1.000 0.120 3 38556460 missense variant A/C;G snv 1
rs199473291 1.000 0.120 3 38551417 missense variant A/C;G snv 1
rs199473156 1.000 0.080 3 38587545 missense variant A/C;G snv 1
rs41311117 0.882 0.120 3 38550362 missense variant A/C;G;T snv 3.6E-05; 2.0E-03; 1.0E-05 2
rs199473639 1.000 0.080 3 38550469 missense variant A/C;G;T snv 1.6E-05; 4.1E-06; 4.1E-06 1
rs199473144 1.000 0.080 3 38597944 missense variant A/C;G;T snv 4.0E-06 1
rs199473627 1.000 0.040 3 38551258 missense variant A/G snv 1
rs199473105 1.000 0.120 3 38606099 missense variant A/G snv 7.0E-06 1
rs199473141 1.000 0.120 3 38598923 missense variant A/G snv 1
rs45589741 1.000 0.120 3 38566501 missense variant A/G snv 1
rs199473615 0.925 0.120 3 38555742 missense variant A/G snv 1
rs79299226 0.851 0.120 3 38550898 missense variant A/G snv 1
rs199473277 1.000 0.120 3 38554311 missense variant A/G snv 1
rs199473183 1.000 0.120 3 38581149 missense variant A/G snv 2.9E-04 2.8E-05 1