Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs440446 0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs769446 0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 6
rs769450 0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39 5
rs1233347077 0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs199768005 0.882 0.160 19 44909057 missense variant T/A snv 4.5E-04 4.9E-04 4
rs752600356 0.851 0.280 19 44908681 missense variant G/A;C snv 2.3E-05 1.4E-05 4
rs761592007 0.882 0.160 19 44909013 missense variant G/A snv 1.5E-05 4
rs748703149 0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs449647 0.925 0.120 19 44905307 upstream gene variant A/T snv 0.21 2
rs7259620 0.925 0.120 19 44904531 upstream gene variant G/A;C snv 2
rs769452 0.925 0.160 19 44907853 missense variant T/C snv 2.5E-03 1.9E-03 2
rs1081105 1.000 0.080 19 44909698 non coding transcript exon variant A/C snv 3.0E-02 1
rs1167428194 1.000 0.080 19 44908634 missense variant A/C snv 1
rs1270059098 1.000 0.080 19 44906634 synonymous variant C/T snv 4.0E-06 1
rs1424027593 1.000 0.080 19 44908639 missense variant C/A snv 1
rs1438607869 1.000 0.080 19 44908741 missense variant G/A snv 1
rs1440976751 1.000 0.080 19 44907789 missense variant G/A snv 1
rs533904656 1.000 0.080 19 44907768 missense variant G/A;C snv 1.8E-04; 8.2E-06 1
rs759721023 1.000 0.080 19 44908936 missense variant G/A snv 8.4E-05 6.3E-05 1
rs981058595 1.000 0.080 19 44908847 missense variant C/A snv 1