Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710
MAGEL2
0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs1352010373
TMEM94
0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs267606826
FOXG1
0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs1060505041
NACC1
0.716 0.400 19 13136099 missense variant C/A;T snv 34
rs137852981
ZEB2
0.752 0.480 2 144399104 stop gained G/A snv 30
rs1064795559
MORC2
0.752 0.320 22 30946373 missense variant G/A snv 29
rs1060499548
ABL1
0.724 0.440 9 130872961 missense variant G/A snv 27
rs180177135
PALB2
0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs397517148
SOS1
0.776 0.200 2 39023128 missense variant C/T snv 27
rs112550005
FBN1
0.742 0.240 15 48425829 stop gained G/A snv 18
rs886039799
BBS9
0.763 0.320 7 33273896 frameshift variant C/- del 17
rs1569525894
SLC9A6
0.790 0.280 X 136040055 frameshift variant TCTTCCTTAACCACCGC/- delins 14
rs786204858
PTEN
0.776 0.280 10 87933079 missense variant A/G;T snv 11
rs1085307138
PUF60 ; SCRIB
0.807 0.160 8 143817591 splice donor variant C/T snv 9
rs875989777
CTSA
0.851 0.320 20 45894704 frameshift variant AT/- delins 9
rs1057518813
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102873305 frameshift variant CT/- delins 8
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 8
rs1057518681
PUF60 ; SCRIB
0.827 0.200 8 143816821 splice acceptor variant T/C snv 7
rs1057518909
FBN1
0.925 0.120 15 48534099 frameshift variant CATT/- delins 5
rs1085307137
PUF60
0.851 0.160 8 143818408 missense variant C/T snv 7.0E-06 5
rs1569146993
TCF20
0.851 0.320 22 42211700 frameshift variant -/C delins 5
rs1064795388
PUF60 ; LOC107986985 ; NRBP2
0.882 0.080 8 143829279 splice donor variant C/G;T snv 3
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53