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
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 16
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 14
rs587777512
LRBA ; MAB21L2
0.827 0.320 4 150583180 missense variant C/G;T snv 6
rs104893915
SLC26A2
0.776 0.200 5 149980428 missense variant C/T snv 9.8E-04 1.0E-03 6
rs774568856
PGM3
0.882 0.200 6 83174481 missense variant A/G snv 1.7E-05 7.0E-06 4
rs886044555
COL2A1
0.925 0.080 12 47985772 missense variant C/T snv 3
rs74315304
CTSK
0.925 0.120 1 150799228 missense variant G/A;T snv 4.0E-06; 4.0E-06 3
rs104893924
SLC26A2
0.851 0.120 5 149981550 missense variant T/A snv 1.1E-04 1.3E-04 1