Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646156 X 15578920 intron variant A/T snv 2
rs146243018 18 22200698 missense variant C/G snv 2.5E-04 1.7E-04 1
rs370588269 8 11756964 missense variant G/A snv 2.4E-05 7.0E-05 1
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs3742264 0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs63751001 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 13
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs72653772 0.807 0.320 16 16190246 missense variant C/T snv 8.4E-05 1.1E-04 16
rs72653744 0.807 0.320 16 16163009 stop gained G/A snv 1.7E-04 1.2E-04 14
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs72650700 0.827 0.240 16 16190247 stop gained G/A;T snv 4.4E-05; 4.0E-06 12
rs72664209 0.827 0.240 16 16173283 splice donor variant C/A snv 8.0E-06; 1.2E-04 1.7E-04 12
rs7667298
KDR
0.827 0.120 4 55125564 5 prime UTR variant T/C snv 0.48 7
rs28939702 0.851 0.320 16 16154899 missense variant G/A;T snv 8.2E-05 13
rs63750459 0.851 0.320 16 16163110 missense variant G/A snv 6.8E-05 6.3E-05 13
rs72653762 0.851 0.240 16 16202006 missense variant T/C snv 5.6E-03 4.7E-03 13
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs72650699 0.851 0.280 16 16202045 stop gained G/A snv 4.8E-05 1.8E-04 12
rs63749856 0.851 0.200 16 16155010 missense variant C/T snv 4.8E-05 2.8E-05 11
rs63750759 0.851 0.280 16 16154974 missense variant G/A;T snv 1.9E-04; 5.4E-06 11
rs63751241 0.882 0.280 16 16154638 missense variant C/T snv 4.0E-05 1.4E-05 12