Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1899663
HOTAIR
0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 17
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 16
rs2107425
MRPL23 ; H19
0.732 0.280 11 1999845 intron variant C/T snv 16
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 8
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 8