Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011121
LOC105371345
16 75292035 downstream gene variant A/C;G snv 1
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1050316
MEF2D
1 156464911 3 prime UTR variant G/T snv 0.54 3
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs10774231 12 4406208 downstream gene variant T/C snv 0.51 1
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 10
rs1163944538
TMEM94
0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1178187217
DNAH11
0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 38
rs12134493 0.925 0.040 1 115135325 TF binding site variant C/A snv 9.2E-02 4
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs12740679 1 150289855 upstream gene variant C/G snv 0.25 1
rs130060
LOC105377864 ; HTR1B
6 77463033 missense variant A/C;G snv 9.9E-03; 4.0E-06 1
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs1441937959
EFL1
0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 20
rs150299874
L2HGDH
1.000 0.120 14 50302901 splice donor variant C/T snv 1.2E-05 7.0E-06 5
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs1555132
NOL4L
20 32458764 intron variant C/A snv 0.44 1
rs1555639076
BPTF
0.790 0.400 17 67893677 splice donor variant A/- delins 16
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs1563452941
SLC20A2
0.882 0.120 8 42437137 stop gained C/A snv 13
rs1564691414
FAS
0.925 0.160 10 89007698 splice acceptor variant A/G snv 7
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs17220352
ASTN2
9 116485780 intron variant A/G snv 0.21 1
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95