Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 2
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 2
rs10497655
LOC105373780 ; ZNF804A
1.000 0.040 2 184597314 intron variant T/C;G snv 1
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 1
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 1
rs2289195
DNMT3A
1.000 0.040 2 25240614 intron variant G/A snv 0.41 0.41 1
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 1
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 1
rs4130047
RIT2
0.925 0.080 18 43098270 intron variant T/A;C snv 1
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 1
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 1
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 1
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 1
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 11