Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553538917
SATB2
0.882 0.120 2 199272423 stop gained G/A snv 7
rs1057518914
RPS6KA3
0.790 0.160 X 20193547 missense variant G/C snv 14
rs121908425
EVC ; CRMP1
0.763 0.160 4 5748226 stop gained C/A;T snv 3.2E-05; 1.2E-05 14
rs753317536
EVC
0.790 0.160 4 5719239 intron variant G/A;C snv 8.0E-06; 4.0E-06 12
rs730882245
KIAA1109
0.827 0.160 4 122207168 stop gained T/A snv 6
rs797045954
SF3B4
0.851 0.160 1 149923568 frameshift variant TCGAGGGGGAACTGGTGGCC/- delins 5
rs1555731819
KMT2B
0.807 0.200 19 35729980 missense variant G/T snv 26
rs1566785444
IRF2BPL
0.827 0.200 14 77025671 frameshift variant C/- delins 20
rs875989803
DDX3X
0.827 0.200 X 41343249 stop gained G/T snv 15
rs1569309484
RLIM
0.807 0.200 X 74591586 missense variant A/G snv 13
rs1057518681
PUF60 ; SCRIB
0.827 0.200 8 143816821 splice acceptor variant T/C snv 7
rs1555398673
FBN1
0.807 0.200 15 48488433 missense variant A/G snv 7
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs794727931
ALG8
0.790 0.240 11 78112692 missense variant A/C snv 19
rs112550005
FBN1
0.742 0.240 15 48425829 stop gained G/A snv 18
rs398122394
ALG13
0.763 0.240 X 111685040 missense variant A/G snv 17
rs61752129
PEX26
0.776 0.240 22 18078405 frameshift variant C/-;CC delins 14
rs397515789
FBN1
0.776 0.240 15 48488112 splice donor variant C/A;T snv 10
rs1057519381
MED12
0.851 0.240 X 71124276 missense variant G/A snv 6
rs1481733213
ATR
0.851 0.240 3 142568059 splice region variant T/C snv 5
rs1553761113
ATR
0.851 0.240 3 142507967 missense variant C/A snv 5
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs864309487
GMNN
0.763 0.280 6 24777279 frameshift variant TCAA/- delins 20
rs797045412
BICD2
0.776 0.280 9 92718565 missense variant G/A;T snv 17
rs1563686762
RAD21 ; UTP23
0.790 0.280 8 116847620 inframe deletion GTT/- delins 16