Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs2420946
FGFR2
0.851 0.160 10 121591810 intron variant T/C snv 0.56 4
rs2981575
FGFR2
0.882 0.120 10 121586602 intron variant G/A snv 0.54 4
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins 4
rs3750817
FGFR2
0.851 0.080 10 121573063 intron variant C/G;T snv 4
rs779848635
FGFR2
0.925 0.080 10 121565562 missense variant C/A;T snv 8.0E-06 4
rs10736303
FGFR2
0.882 0.120 10 121574943 intron variant G/A snv 0.40 3
rs1078806
FGFR2
0.925 0.080 10 121579461 intron variant A/G;T snv 0.34 2
rs1296941849
FGFR2
0.925 0.080 10 121496653 missense variant G/A snv 4.0E-06 2
rs2912774
FGFR2
0.925 0.080 10 121589148 intron variant T/A;G snv 2
rs2981578
FGFR2
0.925 0.080 10 121580797 intron variant C/A;T snv 2
rs746116691
FGFR2
0.925 0.080 10 121515162 synonymous variant A/G;T snv 4.0E-06 2
rs774554190
FGFR2
0.925 0.080 10 121593750 missense variant G/A;T snv 4.0E-06 2
rs7895676
FGFR2
0.925 0.080 10 121574483 intron variant C/T snv 0.40 2
rs1219642
FGFR2
1.000 0.080 10 121588875 intron variant T/C snv 0.41 1
rs2936870
FGFR2
1.000 0.080 10 121589388 intron variant T/C snv 0.54 1