Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778139192
KIF7 ; TICRR
0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 14
rs750195040
POMT1
0.827 0.160 9 131506164 inframe deletion CTT/- delins 3.2E-05 7.0E-06 12
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 11
rs1057516033
KAT6B
0.807 0.400 10 75025250 splice donor variant G/A snv 9
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 9
rs431905509
SLC25A1
0.807 0.280 22 19176222 missense variant G/A;C snv 2.0E-05 8
rs1064796460
TUBA1A
0.790 0.400 12 49185197 missense variant C/G;T snv 8
rs1555696625
NFIX
0.851 0.360 19 13025409 missense variant G/A snv 7
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs886039811
B9D1
0.807 0.320 17 19357875 missense variant A/G snv 4.0E-06 6
rs1555155556
BORCS5
0.851 0.120 12 12435627 splice acceptor variant G/T snv 6
rs1057518951
ARID1B
0.827 0.160 6 156829296 stop gained C/T snv 5
rs797045277
ARID1B
0.882 0.280 6 157198907 splice region variant G/A snv 5
rs1555682265
DCC
0.851 0.160 18 52923796 frameshift variant TTTCTGG/- delins 5
rs1569234334
KIF4A
0.851 0.200 X 70329420 missense variant G/T snv 5
rs1555380716
SLC12A6
0.882 0.120 15 34255385 frameshift variant -/C delins 5
rs1563406024
FZD3
0.851 0.240 8 28555799 frameshift variant -/A delins 4
rs797045005
TUBA1A
0.851 0.320 12 49185140 missense variant A/G snv 4
rs1563183469
AUTS2
0.925 0.120 7 70766245 missense variant A/C snv 3
rs1558519119
BCL11A
0.925 0.120 2 60546061 frameshift variant C/- del 3
rs750610248
BCL11B
0.882 0.200 14 99175513 missense variant A/C;G snv 4.1E-06 3
rs754914260
DCC
0.925 0.120 18 52923832 stop gained C/A;T snv 4.0E-06 3
rs121907917
PAX6
0.807 0.240 11 31794079 stop gained G/A snv 3
rs1057523157
SETD2
0.925 0.120 3 47088172 missense variant G/A snv 3
rs1057517858
TUBA1A
0.925 0.240 12 49185714 missense variant C/A;T snv 3