Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 9
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs2248137
CYP24A1
0.827 0.160 20 54173204 intron variant C/G snv 0.49 5
rs3828599
GPX3 ; LOC105378228
0.882 0.040 5 151022235 intron variant A/G snv 0.67 5
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs11175834
LINC02454 ; LOC100507065
0.925 0.080 12 65598856 intron variant C/T snv 0.14 2
rs1220597
SPATA13
0.925 13 24243875 intron variant C/T snv 0.51 2
rs12990503
DIRC3
0.925 0.080 2 217429494 intron variant C/G snv 0.64 2
rs13184587
ARSB
0.925 5 78910960 intron variant G/A;T snv 2
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs3136166
ERCC4
0.925 16 13938236 intron variant T/G snv 0.44 2
rs4649295
PCNX2
0.925 0.080 1 233280792 intron variant T/C snv 0.60 2
rs6996585
NRG1
0.925 0.080 8 32543285 intron variant A/G snv 0.37 2
rs9858271
LOC105377110
0.925 0.080 3 59559604 intron variant G/A snv 0.80 2
rs2480258
CYP2E1
1.000 10 133538596 intron variant T/C snv 0.63 1
rs34081947
LOC105370451 ; LINC00609
1.000 14 36090325 intron variant C/T snv 0.44 1
rs10136427
LOC105370572
0.925 14 75513546 intergenic variant C/T snv 0.21 2
rs16962916 0.925 16 13806476 intergenic variant A/C;G snv 2