Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2237895 0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1223231582 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2195239 0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1693482 0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53