Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38