Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805010 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3763309 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs37972 0.851 0.160 7 7967878 3 prime UTR variant T/A;C snv 5
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223