Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6150410 0.925 0.040 7 155454910 intron variant CGCATCCCC/-;CGCATCCCCCGCATCCCC delins 0.28 2
rs6735330
XPO1
0.925 0.040 2 61504343 intron variant G/A snv 0.18 2
rs6950765
WNT2
0.925 0.040 7 117281176 intron variant C/G snv 0.64 2
rs7122539
PC
0.925 0.040 11 66895260 intron variant G/A snv 0.43 2
rs7170637
CYFIP1
0.925 0.040 15 22903836 missense variant C/T snv 0.18 0.30 2
rs7294536
AVPR1A
0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
rs745638189
PTEN
1.000 0.040 10 87960997 missense variant G/A snv 4.0E-06 7.0E-06 2
rs747756965
DNAH8
0.925 0.040 6 38775924 missense variant T/A;C snv 4.0E-06 2
rs748128078
GRIN2B
0.925 0.040 12 13562968 missense variant G/A snv 1.6E-05 5.6E-05 2
rs751945904
NLGN4X
0.925 0.040 X 5893158 missense variant G/A snv 1.1E-05 2
rs756472
MRTFB
0.925 0.040 16 14185624 intron variant G/A snv 0.24 2
rs756790727
GRIN2B
0.925 0.040 12 13562883 missense variant G/A snv 1.2E-05 2
rs7603001
ZNF804A
0.925 0.040 2 184902089 intron variant A/G;T snv 2
rs7608798
DPP4
0.925 0.040 2 162033707 intron variant G/A snv 0.35 2
rs879254129
GRIN2B
0.925 0.040 12 13562977 missense variant A/G snv 4.0E-06 2
rs9635542
PPL
1.000 0.040 16 4951379 intron variant A/G snv 0.11 2
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs10185592
LOC105373847
1.000 0.040 2 205829457 intergenic variant A/C snv 0.11 1
rs10205350
GALNT14
1.000 0.040 2 30923631 intron variant G/T snv 0.24 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10489525
CSDE1
1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10500171
CNTNAP2
1.000 0.040 7 147183313 intron variant A/G snv 0.52 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs1053972
KLK3
1.000 0.040 19 50855373 3 prime UTR variant C/T snv 0.24 1