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
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
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
rs374608214
FGFR2
0.742 0.160 10 121520010 missense variant G/C snv 4.0E-06 7.0E-06 13
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 13
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 9
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 9
rs121909627
FGFR1
0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 8
rs121918497
FGFR2
0.776 0.160 10 121520052 missense variant T/G snv 8
rs121918488
FGFR2
0.790 0.120 10 121517379 missense variant A/C;G;T snv 7
rs121918490
FGFR2
0.851 0.080 10 121517342 missense variant G/C snv 6
rs121918501
FGFR2
0.807 0.080 10 121520050 missense variant A/C;G snv 6
rs121909631
FGFR1
0.827 0.280 8 38419696 missense variant T/C snv 5
rs746082633
FGFR1
0.827 0.280 8 38418270 missense variant T/C snv 1.6E-05 1.4E-05 5
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 5
rs1057519043
FGFR2
0.851 0.120 10 121517391 missense variant C/A;G;T snv 4
rs121918496
FGFR2
0.851 0.120 10 121517377 missense variant G/C snv 4
rs777169135
FGFR2
0.851 0.080 10 121488064 missense variant T/C;G snv 4.0E-06 4
rs1057519038
FGFR2
0.882 0.120 10 121520076 missense variant T/C snv 3
rs121918492
FGFR2
0.882 0.080 10 121517372 missense variant G/C snv 7.0E-06 3
rs121918507
FGFR2
0.882 0.280 10 121498591 missense variant T/C snv 3
rs974173968
FGFR2
0.882 0.080 10 121551382 missense variant G/A;T snv 8.0E-06 3
rs1285894726
TGM2
0.882 0.120 20 38141329 missense variant T/C snv 3
rs1265366960
FGFR2
0.925 0.080 10 121503857 missense variant G/C snv 7.0E-06 2