Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 3
rs121918506
FGFR2
0.882 0.080 10 121496701 missense variant T/C;G snv 3
rs879253721
FGFR2
0.925 0.080 10 121517316 splice region variant T/C snv 2
rs1057519047
FGFR2
1.000 0.080 10 121488055 missense variant T/C;G snv 1
rs121918495
FGFR2
0.925 0.080 10 121517382 missense variant T/G snv 1
rs121918501
FGFR2
0.807 0.080 10 121520050 missense variant A/C;G snv 1
rs121918503
FGFR2
1.000 0.080 10 121520098 inframe deletion GTC/- delins 1
rs121918510
FGFR2
1.000 0.080 10 121517441 missense variant T/G snv 1
rs1358919643
FGFR2
1.000 0.080 10 121517463 missense variant C/A;T snv 4.0E-06 1
rs879253719
FGFR2
1.000 0.080 10 121517464 splice acceptor variant C/T snv 1
rs886037837
FGFR2
1.000 0.080 10 121520037 inframe deletion CGTGCTTGATCCACTGGA/- delins 1
rs776587763
FGFR2
0.790 0.120 10 121520085 missense variant C/A;T snv 4.0E-06; 4.0E-06 6
rs121918488
FGFR2
0.790 0.120 10 121517379 missense variant A/C;G;T snv 4
rs1057519037
FGFR2
0.925 0.120 10 121520084 missense variant GC/AA;TA mnv 2
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 4
rs121918497
FGFR2
0.776 0.160 10 121520052 missense variant T/G snv 3
rs1057519041
FGFR2
0.925 0.160 10 121517465 splice acceptor variant T/C snv 2
rs121918499
FGFR2
0.925 0.160 10 121520048 missense variant C/A;G snv 2
rs121909627
FGFR1
0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 3
rs1554552774
FGFR1
0.925 0.200 8 38418227 splice donor variant C/T snv 2
rs1554570706
FGFR1
0.925 0.200 8 38429808 missense variant G/A snv 2
rs1554570813
FGFR1
0.925 0.200 8 38429826 stop gained G/A snv 2
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 3
rs121918487
FGFR2
0.716 0.440 10 121517378 missense variant C/A;G;T snv 24
rs121918491
FGFR2
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 14