Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs696 0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49