Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 12
rs121909641
FGFR1
0.763 0.520 8 38419720 missense variant G/A snv 9
rs121909627
FGFR1
0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 8
rs121909636
FGFR1
0.827 0.240 8 38414569 stop gained G/A snv 7
rs397515445
FGFR1
0.807 0.280 8 38414263 missense variant T/C snv 7
rs1057519897
FGFR1
0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 6
rs121909635
FGFR1
0.827 0.240 8 38426158 missense variant C/T snv 6
rs1057519898
FGFR1
0.851 0.120 8 38417333 missense variant T/C snv 5
rs1057519899
FGFR1
0.851 0.120 8 38417879 missense variant T/C snv 5
rs121909631
FGFR1
0.827 0.280 8 38419696 missense variant T/C snv 5
rs267606805
FGFR1
0.851 0.240 8 38414173 missense variant G/T snv 5
rs267606806
FGFR1
0.851 0.240 8 38414166 missense variant G/A;C snv 1.2E-05 5
rs746082633
FGFR1
0.827 0.280 8 38418270 missense variant T/C snv 1.6E-05 1.4E-05 5
rs1306185959
FGFR1
0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs1458235863
FGFR1
0.925 0.160 8 38412424 3 prime UTR variant G/A snv 5.6E-05 4
rs121909628
FGFR1
0.925 0.160 8 38414892 stop gained G/A;C snv 3
rs121909629
FGFR1
0.882 0.200 8 38415905 missense variant C/T snv 3
rs121909637
FGFR1
0.882 0.240 8 38418249 missense variant C/A;T snv 1.2E-05; 2.0E-05 3
rs121909638
FGFR1
0.882 0.280 8 38421853 missense variant A/G snv 3
rs13317
FGFR1
0.882 0.120 8 38411996 3 prime UTR variant T/C snv 0.23 3
rs515726224
FGFR1
0.925 0.320 8 38417962 missense variant C/T snv 3
rs557263543
FGFR1
8 38412508 3 prime UTR variant C/T snv 3
rs727505369
FGFR1
0.925 0.160 8 38424624 missense variant T/C snv 3
rs727505373
FGFR1
0.925 0.160 8 38429744 missense variant T/C snv 3