Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10937405 0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs13042395 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs314276 0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3782130 0.925 0.120 12 57768115 intron variant G/A;C snv 0.27 4
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4645981 0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs667282 0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs6682925 0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10