Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs1161457931
TMPRSS6
0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs1248696
DLG5
0.807 0.080 10 77856847 missense variant T/A;C snv 0.93 8
rs1554893835
PTEN
0.827 0.240 10 87894110 splice donor variant G/C;T snv 8
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs1085308051
PTEN
0.882 0.200 10 87933229 missense variant A/G snv 4.0E-06 6
rs1545620
MYO9B
0.827 0.080 19 17192965 missense variant T/A;G snv 1.3E-05; 0.52 6
rs199474387
HLA-A
0.807 0.240 6 29942870 missense variant G/C;T snv 6
rs11552708
TNFSF12-TNFSF13 ; TNFSF13
0.882 0.240 17 7559238 missense variant G/A;C snv 0.13; 4.2E-06 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5