Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3824260
CYP7A1
0.742 0.160 8 58500631 upstream gene variant A/G;T snv 11
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs121434254
AIRE
0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 6
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs12373142
SPPL2C ; MAPT-AS1
0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 5
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs582054
IL12A ; IL12A-AS1
0.882 0.160 3 159992214 intron variant A/C;T snv 5
rs12185233
SPPL2C ; MAPT-AS1
0.882 0.160 17 45846288 missense variant G/A;C snv 9.5E-05; 0.15 4
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 4
rs2075533
DELEC1 ; TNFSF8
0.851 0.160 9 114931351 intron variant G/A;T snv 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs12936231
ZPBP2
0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs199525
WNT3 ; LRRC37A2
1.000 0.080 17 46770468 intron variant T/A;G snv 3
rs473351
ABCB11
0.925 0.120 2 168923386 3 prime UTR variant T/A;C;G snv 3