Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1057516230
ALPL
0.925 0.080 1 21554124 frameshift variant AACT/- delins 2
rs1057518967
COL1A2
1.000 0.040 7 94423102 missense variant G/A snv 2
rs116571438
TRPV4
0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 2
rs1209546147
COL2A1 ; LOC105369752
1.000 0.040 12 47980597 missense variant C/T snv 1
rs121912632
TRPV4
0.882 0.080 12 109792407 missense variant C/T snv 3
rs121912633
TRPV4
0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs121912634
TRPV4
0.925 0.080 12 109798768 missense variant T/C snv 2
rs121912635
TRPV4
0.925 0.080 12 109788462 missense variant C/A snv 2
rs121912636
TRPV4
0.925 0.120 12 109798775 missense variant T/A;C snv 4.0E-06 2
rs121912637
TRPV4
0.851 0.160 12 109784378 missense variant G/A;C snv 5
rs121913105
FGFR3
0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs121918130
INPP5E
0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 18
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs1400419650
TRIP11
0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022
TRIP11
0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs181011657
DYNC2H1
0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 3
rs267607147
TRPV4
0.925 0.120 12 109784379 missense variant G/A;C snv 2
rs267607148
TRPV4
0.882 0.120 12 109800639 missense variant C/T snv 4
rs267607149
TRPV4
0.851 0.120 12 109784385 missense variant C/T snv 5
rs267607150
TRPV4
0.925 0.080 12 109792671 missense variant T/C snv 2
rs28933068
FGFR3
0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs369091875
DCHS1
0.925 0.240 11 6633485 missense variant C/G;T snv 1.1E-03 2
rs369634007
TMEM87B
0.882 0.080 2 112098688 missense variant A/G snv 1.6E-05 2.1E-05 10