Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 27
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 19
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 16
rs374608214
FGFR2
0.742 0.160 10 121520010 missense variant G/C snv 4.0E-06 7.0E-06 13
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 7
rs121918497
FGFR2
0.776 0.160 10 121520052 missense variant T/G snv 7
rs121918501
FGFR2
0.807 0.080 10 121520050 missense variant A/C;G snv 6
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 6
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 6
rs121918487
FGFR2
0.716 0.440 10 121517378 missense variant C/A;G;T snv 5
rs121918488
FGFR2
0.790 0.120 10 121517379 missense variant A/C;G;T snv 5
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 5
rs2420946
FGFR2
0.851 0.160 10 121591810 intron variant T/C snv 0.56 4
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins 4
rs779848635
FGFR2
0.925 0.080 10 121565562 missense variant C/A;T snv 8.0E-06 4
rs3750817
FGFR2
0.851 0.080 10 121573063 intron variant C/G;T snv 4
rs121918496
FGFR2
0.851 0.120 10 121517377 missense variant G/C snv 4
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 4
rs776587763
FGFR2
0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs10736303
FGFR2
0.882 0.120 10 121574943 intron variant G/A snv 0.40 3
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 3
rs747718232
FGFR2
1.000 0.120 10 121488017 missense variant T/C snv 4.0E-06 3
rs974173968
FGFR2
0.882 0.080 10 121551382 missense variant G/A;T snv 8.0E-06 3
rs121918490
FGFR2
0.851 0.080 10 121517342 missense variant G/C snv 3