Source: ALL
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
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
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
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
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 21
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17