Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867120336 1.000 0.040 2 10048589 frameshift variant -/A delins 4.1E-06 2
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs36217263
KL
1.000 0.040 13 33015697 upstream gene variant A/- del 0.21 4
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs3134069 0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs4833103 0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs113296370 1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs16860234 0.925 0.080 3 185793096 intron variant A/C snv 0.33 3
rs2275703 0.925 0.080 1 160195305 intron variant A/C snv 0.38 3
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs497309 0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs2542713
DAB2 ; C9
1.000 0.040 5 39385539 intron variant A/C;G snv 3
rs2236513 1.000 0.040 17 17844052 3 prime UTR variant A/C;G snv 0.58 2
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs779271027 1.000 0.040 20 44413723 missense variant A/C;G snv 4.0E-06; 8.0E-06 2
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1042615 1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97