Source: BEFREE

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 10
rs121909627
FGFR1
0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 6
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 6
rs397515445
FGFR1
0.807 0.280 8 38414263 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
rs267606806
FGFR1
0.851 0.240 8 38414166 missense variant G/A;C snv 1.2E-05 5
rs121909636
FGFR1
0.827 0.240 8 38414569 stop gained G/A snv 5
rs267606805
FGFR1
0.851 0.240 8 38414173 missense variant G/T snv 5
rs121909635
FGFR1
0.827 0.240 8 38426158 missense variant C/T snv 5
rs1458235863
FGFR1
0.925 0.160 8 38412424 3 prime UTR variant G/A snv 5.6E-05 4
rs121909631
FGFR1
0.827 0.280 8 38419696 missense variant T/C snv 4
rs1306185959
FGFR1
0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs557263543
FGFR1
8 38412508 3 prime UTR variant C/T snv 3
rs756016701
FGFR1
0.882 0.080 8 38419718 missense variant C/A snv 4.0E-06 3
rs981703846
FGFR1
0.882 0.080 8 38421872 missense variant C/A;T snv 8.0E-06 3
rs17182023
FGFR1
0.925 0.080 8 38469497 upstream gene variant C/T snv 0.28 2
rs375611478
FGFR1
8 38414584 missense variant G/A snv 4.0E-06 1.4E-05 2
rs121909637
FGFR1
0.882 0.240 8 38418249 missense variant C/A;T snv 1.2E-05; 2.0E-05 2
rs780153672
FGFR1
0.925 0.160 8 38428352 missense variant G/A snv 2.8E-05 2.1E-05 2
rs886042254
FGFR1
0.925 0.160 8 38428079 missense variant A/G snv 2
rs747333248
FGFR1
0.925 0.160 8 38418234 missense variant C/T snv 2.4E-05 1.4E-05 2
rs372654433
FGFR1
0.925 0.200 8 38418339 missense variant C/T snv 4.0E-05 2.8E-05 2
rs374473310
FGFR1
0.925 0.200 8 38413943 missense variant C/T snv 2.0E-05 2.1E-05 2
rs746602135
FGFR1
0.925 0.160 8 38413746 missense variant C/T snv 3.2E-05 4.9E-05 2
rs752627281
FGFR1
1.000 8 38419631 missense variant C/T snv 2.4E-05 6.3E-05 1