Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 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
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 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
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 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
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7