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
rs121912633
TRPV4
0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 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
rs121912632
TRPV4
0.882 0.080 12 109792407 missense variant C/T snv 2
rs387906904
TRPV4
0.851 0.080 12 109803009 missense variant G/A snv 1
rs77975504
TRPV4
0.827 0.280 12 109792695 missense variant C/T snv 1