Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227948
MCC
0.925 0.120 5 113043592 synonymous variant G/A;T snv 0.53; 4.0E-06 2
rs1050171 0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs222836 0.925 0.120 17 7229843 synonymous variant G/A snv 0.51 0.47 2
rs1051624 1.000 0.080 8 94130944 missense variant T/A;G snv 2.0E-05; 0.51 1
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs515746 1.000 0.080 12 114681192 intron variant G/A snv 0.49 0.48 1
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs2306283 0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs8100241 0.827 0.120 19 17282085 missense variant G/A snv 0.47 0.47 5
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2976392
JRK ; PSCA
0.724 0.240 8 142681514 3 prime UTR variant G/A snv 0.46 0.45 15
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs12979278 0.790 0.080 19 48715345 synonymous variant C/T snv 0.46 0.40 9
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs2070699 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 14
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs4586 0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8