Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42