Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4647924
FGFR3
0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs28931614
FGFR3
0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs121913116
FGFR3
0.763 0.360 4 1799395 missense variant C/T snv 9
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs1211533350
FGFR3
0.827 0.120 4 1805638 synonymous variant C/A snv 4.0E-06 7.0E-06 5
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs1057520029
FGFR2
0.925 0.120 10 121488003 missense variant T/A snv 4
rs4846913
GALNT2
1.000 0.120 1 230158968 intron variant C/A;T snv 4
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 4
rs747718232
FGFR2
1.000 0.120 10 121488017 missense variant T/C snv 4.0E-06 3
rs267606808
FGFR3
0.882 0.120 4 1805396 missense variant A/G snv 3
rs7552841
PCSK9
0.925 0.160 1 55053079 intron variant C/T snv 0.32 3
rs869025672
FGFR1
0.925 0.320 8 38414872 missense variant A/C;G snv 8.0E-06 2
rs121913114
FGFR3
0.925 0.120 4 1801930 missense variant A/G;T snv 4.0E-06 2
rs121913115
FGFR3
1.000 0.120 4 1801928 missense variant A/G snv 2
rs28928868
FGFR3
0.925 0.120 4 1806164 missense variant G/C;T snv 4.0E-06 2
rs80053154
FGFR3
0.925 0.120 4 1805636 missense variant A/G snv 1.2E-05 7.0E-06 2