Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912633
TRPV4
0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs749621890
EXTL3
0.851 0.040 8 28717012 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs515726167
TRPV4
0.925 0.120 12 109803106 missense variant C/G;T snv 4.0E-06 2
rs751994699
ALPL
1.000 0.040 1 21563170 frameshift variant GG/- delins 4.0E-06 2.1E-05 1
rs1400419650
TRIP11
0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs759549373
DYNC2H1
0.925 0.080 11 103253342 missense variant G/A;T snv 6.0E-05; 4.0E-06 4
rs121918130
INPP5E
0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 18
rs116571438
TRPV4
0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 2
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs369634007
TMEM87B
0.882 0.080 2 112098688 missense variant A/G snv 1.6E-05 2.1E-05 10
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs774568856
PGM3
0.882 0.200 6 83174481 missense variant A/G snv 1.7E-05 7.0E-06 4
rs181011657
DYNC2H1
0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 3
rs369091875
DCHS1
0.925 0.240 11 6633485 missense variant C/G;T snv 1.1E-03 2