Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs1805377 0.689 0.480 5 83353124 splice acceptor variant G/A snv 0.23 0.25 19
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs5743551 0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131