Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909627
FGFR1
0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 8
rs121918488
FGFR2
0.790 0.120 10 121517379 missense variant A/C;G;T snv 7
rs776587763
FGFR2
0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 7
rs121918504
FGFR2
0.807 0.120 10 121517460 missense variant C/A;T snv 2.4E-05 9
rs771148519
WDR19
0.807 0.200 4 39225027 stop gained C/G snv 1.7E-05 1.4E-05 9
rs34210653
ALOX15
0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 8
rs37973
GLCCI1 ; GLCCI1-DT
0.807 0.280 7 7968245 intron variant G/A;C snv 7
rs121918501
FGFR2
0.807 0.080 10 121520050 missense variant A/C;G snv 6
rs140598
FBN1
0.827 0.160 15 48487333 missense variant G/A;C snv 3.2E-02 5
rs28933372
GLI3
0.827 0.120 7 41966273 missense variant C/G snv 5
rs786200952
KAT6A
0.851 0.120 8 41934340 frameshift variant -/T delins 13
rs10246939
TAS2R38 ; MGAM
0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 6
rs1554442015
TWIST1
0.851 0.120 7 19116970 missense variant G/C snv 5
rs121908671
LRP5
0.851 0.120 11 68357801 missense variant G/A snv 4
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 4
rs777169135
FGFR2
0.851 0.080 10 121488064 missense variant T/C;G snv 4.0E-06 4
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 4
rs1060499549
ZNF462
0.882 0.120 9 106927699 stop gained C/T snv 4
rs886043448
DNAH5
0.882 0.200 5 13793709 missense variant C/T snv 2.0E-05 1.4E-05 4
rs104893895
MSX2
0.882 0.160 5 174729222 missense variant C/A;T snv 3
rs121913113
FGFR3
0.882 0.240 4 1806076 missense variant G/A snv 3
rs121918506
FGFR2
0.882 0.080 10 121496701 missense variant T/C;G snv 3
rs756016701
FGFR1
0.882 0.080 8 38419718 missense variant C/A snv 4.0E-06 3
rs766812325
RUNX2
0.882 0.080 6 45492058 missense variant C/G snv 3