Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867114783 17 7675109 missense variant T/C snv 5
rs7668666 1.000 4 186080138 intron variant C/A;T snv 4
rs11121704 1 11233902 intron variant C/A;T snv 3
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1156560901 2 201880120 missense variant A/G snv 1.4E-05 2
rs1212415280 6 43771130 missense variant G/T snv 2.1E-05 2
rs1308088661 17 39727880 missense variant G/A snv 4.0E-06 2
rs181264737 8 124589710 missense variant C/A;G;T snv 1.2E-05; 4.1E-06; 4.1E-06 2
rs723526 1.000 7 55067126 intron variant A/G snv 0.86 2
rs753066745 X 81277164 missense variant C/T snv 1.7E-05 9.5E-06 2
rs771308693 8 140752306 missense variant G/A snv 3.2E-05 7.0E-06 2
rs1053129 5 80626901 3 prime UTR variant C/A;T snv 1
rs10964859 9 21140673 3 prime UTR variant C/A;G snv 1
rs10964862 9 21151554 intergenic variant C/A;G snv 1
rs1317052311 X 15358134 missense variant C/A snv 5.5E-06 1
rs1472189 11 11962338 3 prime UTR variant C/T snv 0.25 1
rs148626207 4 102612593 missense variant T/C snv 8.0E-06 1.4E-05 1
rs200246209 11 102527789 synonymous variant G/A snv 8.0E-06 1.4E-05 1
rs2375801 4 186550471 intron variant T/C snv 0.34 1
rs2994809 1 119809354 intron variant T/C snv 0.91 1
rs3206652 3 108046402 3 prime UTR variant T/C snv 0.27 1
rs370006648
NDN
15 23687168 missense variant G/A snv 4.1E-05 7.0E-05 1
rs377767422
RET
10 43119635 missense variant C/T snv 1.2E-05 2.1E-05 1
rs3804639 3 108071988 intron variant G/T snv 0.28 1
rs684559 1 111215824 intron variant G/A snv 0.27 1