Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs7813 0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 16
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 61
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs2072454 0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
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
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187