Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906324
TRPV4
0.925 0.080 12 109808308 missense variant C/T snv 2
rs387906903
TRPV4
0.925 0.120 12 109803113 missense variant T/C snv 2
rs397514473
TRPV4
0.925 0.120 12 109814531 missense variant G/A snv 2
rs515726152
TRPV4
0.925 0.120 12 109798742 missense variant C/A snv 2
rs515726157
TRPV4
1.000 0.040 12 109792704 missense variant T/C snv 2
rs515726158
TRPV4
0.925 0.120 12 109792702 missense variant A/G snv 2
rs515726159
TRPV4
0.925 0.080 12 109792689 missense variant A/G snv 2
rs515726160
TRPV4
0.925 0.080 12 109792678 missense variant C/A snv 2
rs515726161
TRPV4
0.925 0.120 12 109792664 missense variant G/C snv 2
rs515726162
TRPV4
0.925 0.120 12 109792403 missense variant G/T snv 2
rs515726163
TRPV4
0.925 0.120 12 109792401 missense variant A/G 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
rs515726166
TRPV4
1.000 0.040 12 109784362 frameshift variant TCATTCTTGCCCGGGTC/- delins 2
rs515726171
TRPV4
0.925 0.120 12 109798883 missense variant T/C snv 2
rs515726172
TRPV4
0.925 0.120 12 109798774 missense variant A/G snv 2
rs1209546147
COL2A1 ; LOC105369752
1.000 0.040 12 47980597 missense variant C/T snv 1
rs515726153
TRPV4
1.000 0.040 12 109796638 missense variant T/C snv 1
rs515726154
TRPV4
1.000 0.040 12 109794406 inframe deletion AAG/- delins 1
rs515726155
TRPV4
1.000 0.040 12 109793945 inframe insertion -/GGA delins 1
rs515726169
TRPV4
1.000 0.040 12 109800754 missense variant C/G snv 1
rs74315304
CTSK
0.925 0.120 1 150799228 missense variant G/A;T snv 4.0E-06; 4.0E-06 3
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs121912636
TRPV4
0.925 0.120 12 109798775 missense variant T/A;C snv 4.0E-06 2
rs387906902
TRPV4
0.925 0.080 12 109793560 missense variant G/C;T snv 4.0E-06 3