Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918487
FGFR2
0.716 0.440 10 121517378 missense variant C/A;G;T snv 24
rs121918494
FGFR2
0.790 0.160 10 121517363 missense variant G/C snv 24
rs1564919048
FGFR2
0.732 0.280 10 121520106 missense variant C/A snv 23
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs121918491
FGFR2
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 14
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 13
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 12
rs1434545235
FGFR2
0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 11
rs1554927408
FGFR2
0.742 0.480 10 121515254 missense variant C/T snv 11
rs1057519044
FGFR2
0.752 0.440 10 121517390 missense variant C/T snv 11
rs776587763
FGFR2
0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 6
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs121918504
FGFR2
0.807 0.120 10 121517460 missense variant C/A;T snv 2.4E-05 6
rs121918490
FGFR2
0.851 0.080 10 121517342 missense variant G/C snv 5
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 5
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 4
rs121918488
FGFR2
0.790 0.120 10 121517379 missense variant A/C;G;T snv 4
rs1057519043
FGFR2
0.851 0.120 10 121517391 missense variant C/A;G;T snv 3
rs121918506
FGFR2
0.882 0.080 10 121496701 missense variant T/C;G snv 3
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 3
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 3