Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4647924
FGFR3
0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 28
rs121918487
FGFR2
0.716 0.440 10 121517378 missense variant C/A;G;T snv 25
rs28931614
FGFR3
0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 17
rs121918491
FGFR2
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 15
rs1554927408
FGFR2
0.742 0.480 10 121515254 missense variant C/T snv 12
rs1057519044
FGFR2
0.752 0.440 10 121517390 missense variant C/T snv 11
rs1434545235
FGFR2
0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 11
rs121913116
FGFR3
0.763 0.360 4 1799395 missense variant C/T snv 9
rs121918508
FGFR2
0.851 0.360 10 121488035 missense variant C/T snv 4
rs886041251
TP63
0.882 0.360 3 189868614 missense variant C/T snv 3
rs104893887
FGF10
0.925 0.280 5 44310447 stop gained T/A snv 2
rs104893888
FGF10-AS1 ; FGF10
0.925 0.280 5 44388443 missense variant T/G snv 2
rs104893886
FGF10
1.000 0.280 5 44305155 missense variant A/C snv 1
rs1554035469
FGF10
1.000 0.280 5 44305072 missense variant C/T snv 1
rs1554035757
FGF10
1.000 0.280 5 44310455 missense variant A/T snv 1
rs1554035763
FGF10
1.000 0.280 5 44310500 frameshift variant C/- delins 1
rs1554040361
FGF10-AS1 ; FGF10
1.000 0.280 5 44388427 frameshift variant T/- del 1
rs1554040396
FGF10-AS1 ; FGF10
1.000 0.280 5 44388682 start lost T/C snv 1