Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057516033
KAT6B
0.807 0.400 10 75025250 splice donor variant G/A snv 9
rs1057517858
TUBA1A
0.925 0.240 12 49185714 missense variant C/A;T snv 3
rs1057518951
ARID1B
0.827 0.160 6 156829296 stop gained C/T snv 5
rs1057519053
DCC
1.000 0.120 18 52925310 frameshift variant A/- del 2
rs1057519054
DCC
1.000 0.120 18 53386061 missense variant T/G snv 2
rs1057519055
DCC
1.000 0.120 18 53386097 missense variant G/A snv 2
rs1057519056
DCC
1.000 0.120 18 53207746 missense variant G/A;C snv 2
rs1057519057
DCC
1.000 0.120 18 53391876 missense variant G/A snv 2
rs1057523157
SETD2
0.925 0.120 3 47088172 missense variant G/A snv 3
rs1064796460
TUBA1A
0.790 0.400 12 49185197 missense variant C/G;T snv 8
rs11893842
OBSL1 ; INHA
0.925 0.160 2 219572251 intron variant A/G snv 0.45 2
rs1190999960
ZNRD2-AS1 ; ZNRD2 ; FAM89B
0.807 0.240 11 65571690 missense variant G/A snv 9
rs121907917
PAX6
0.807 0.240 11 31794079 stop gained G/A snv 6
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1250394819
LOC101927100 ; TMED7-TICAM2 ; TMED7
0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs1285675735
SORD
0.827 0.200 15 45043384 synonymous variant C/G;T snv 1.1E-05; 1.1E-05 6
rs148634289
SDHD
0.827 0.200 11 112088925 synonymous variant C/T snv 1.6E-05 2.1E-05 6
rs1555155556
BORCS5
0.851 0.120 12 12435627 splice acceptor variant G/T snv 6
rs1555380716
SLC12A6
0.882 0.120 15 34255385 frameshift variant -/C delins 5
rs1555682265
DCC
0.851 0.160 18 52923796 frameshift variant TTTCTGG/- delins 5
rs1555696625
NFIX
0.851 0.360 19 13025409 missense variant G/A snv 7
rs1558519119
BCL11A
0.925 0.120 2 60546061 frameshift variant C/- del 3
rs1563183469
AUTS2
0.925 0.120 7 70766245 missense variant A/C snv 3
rs1563406024
FZD3
0.851 0.240 8 28555799 frameshift variant -/A delins 4
rs1565627707
TUBA1A
0.925 0.240 12 49186657 missense variant C/A snv 3