Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039814
WDR19
0.807 0.200 4 39218060 missense variant C/G snv 13
rs771148519
WDR19
0.807 0.200 4 39225027 stop gained C/G snv 1.7E-05 1.4E-05 9
rs387906980
WDR19
0.807 0.200 4 39231943 missense variant T/C snv 1.2E-05 2.8E-05 6
rs786205567
IFT122
0.925 0.120 3 129500070 splice donor variant T/C snv 5
rs183758503
SPAG17
0.851 0.160 1 118093260 missense variant C/G;T snv 2.0E-04; 1.2E-05 5
rs200140363
WDR35
0.851 0.160 2 19953852 missense variant C/T snv 3.2E-05 2.8E-05 5
rs199952377
WDR35
0.851 0.160 2 19941796 stop gained A/C snv 1.6E-04 1.9E-04 4
rs267607191
IFT122
0.925 0.160 3 129481546 missense variant T/G snv 4.0E-06 2
rs267607192
IFT122
0.925 0.160 3 129476463 missense variant C/T snv 2.8E-05 2
rs376595844
IFT122
0.925 0.160 3 129461309 splice region variant G/A;C;T snv 2.4E-05; 8.0E-06 2
rs267607193
IFT122 ; MBD4
0.925 0.160 3 129440351 missense variant G/C snv 2
rs1417500285
IFT140
0.925 0.240 16 1562007 missense variant G/A snv 1.4E-05 2
rs387906981
WDR19
0.925 0.120 4 39268040 stop gained C/A;T snv 4.3E-06; 1.3E-05 2
rs267607174
WDR35
0.925 0.120 2 19945787 missense variant T/C snv 2
rs267607175
WDR35
0.925 0.120 2 19933469 missense variant C/T snv 4.0E-06 7.0E-06 2
rs397515334
WDR35
0.925 0.120 2 19931375 frameshift variant G/- delins 4.0E-06 2
rs397515533
WDR35
0.925 0.120 2 19946536 missense variant A/G snv 7.0E-06 2
rs397515534
WDR35 ; LOC101928222
0.925 0.120 2 19989284 splice acceptor variant T/C;G snv 8.0E-06 2
rs397515567
IFT122
1.000 0.120 3 129476450 frameshift variant G/- delins 1
rs387907107
IFT43
1.000 0.120 14 75985787 start lost A/G snv 1
rs397515535
WDR35
1.000 0.120 2 19931354 missense variant T/C snv 8.0E-06 1
rs397515536
WDR35
1.000 0.120 2 19975596 missense variant A/T snv 1.4E-05 1