Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 20
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 18
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 11
rs2963
INSR
0.851 0.240 19 7163143 synonymous variant G/A snv 9.8E-02 0.13 4
rs587779383
FGFR3
0.851 0.120 4 1806157 missense variant A/C;G;T snv 3
rs1445362103
ARHGEF7
1.000 0.040 13 111244248 missense variant T/C snv 1.2E-05 7.0E-06 2
rs121913135
INSR
0.882 0.120 19 7125437 missense variant C/A snv 2
rs587777260
TBC1D4
0.925 0.080 13 75359852 stop gained G/A;T snv 4.0E-06 2
rs752411521
CBFA2T2
1.000 0.040 20 33624825 missense variant T/C snv 4.0E-06 1