Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs369091875
DCHS1
0.925 0.240 11 6633485 missense variant C/G;T snv 1.1E-03 2
rs515726167
TRPV4
0.925 0.120 12 109803106 missense variant C/G;T snv 4.0E-06 2
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs77975504
TRPV4
0.827 0.280 12 109792695 missense variant C/T snv 6
rs267607149
TRPV4
0.851 0.120 12 109784385 missense variant C/T snv 5
rs267607148
TRPV4
0.882 0.120 12 109800639 missense variant C/T snv 4
rs886043613
FGFR3
0.925 0.080 4 1801519 missense variant C/T snv 4
rs121912632
TRPV4
0.882 0.080 12 109792407 missense variant C/T snv 3
rs181011657
DYNC2H1
0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 3
rs886044555
COL2A1
0.925 0.080 12 47985772 missense variant C/T snv 3
rs387906324
TRPV4
0.925 0.080 12 109808308 missense variant C/T snv 2
rs515726164
TRPV4
0.925 0.080 12 109792379 missense variant C/T snv 2
rs515726165
TRPV4
0.925 0.080 12 109786716 missense variant C/T snv 2
rs1209546147
COL2A1 ; LOC105369752
1.000 0.040 12 47980597 missense variant C/T snv 1
rs886041093
EHMT1
0.827 0.280 9 137815998 missense variant G/A snv 7
rs387906904
TRPV4
0.851 0.080 12 109803009 missense variant G/A snv 5
rs387906906
TRPV4
0.925 0.120 12 109786827 missense variant G/A snv 3
rs1057518967
COL1A2
1.000 0.040 7 94423102 missense variant G/A snv 2
rs397514473
TRPV4
0.925 0.120 12 109814531 missense variant G/A snv 2
rs121912637
TRPV4
0.851 0.160 12 109784378 missense variant G/A;C snv 5
rs267607147
TRPV4
0.925 0.120 12 109784379 missense variant G/A;C snv 2
rs121918130
INPP5E
0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 18
rs759549373
DYNC2H1
0.925 0.080 11 103253342 missense variant G/A;T snv 6.0E-05; 4.0E-06 4
rs74315304
CTSK
0.925 0.120 1 150799228 missense variant G/A;T snv 4.0E-06; 4.0E-06 3
rs116571438
TRPV4
0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 2