Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315304
CTSK
0.925 0.120 1 150799228 missense variant G/A;T snv 4.0E-06; 4.0E-06 3
rs181011657
DYNC2H1
0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 3
rs869312694
MAGEL2
0.925 0.120 15 23644535 stop gained C/A snv 3
rs121912632
TRPV4
0.882 0.080 12 109792407 missense variant C/T snv 3
rs387906902
TRPV4
0.925 0.080 12 109793560 missense variant G/C;T snv 4.0E-06 3
rs387906906
TRPV4
0.925 0.120 12 109786827 missense variant G/A snv 3
rs387906907
TRPV4
0.925 0.120 12 109800645 missense variant T/C snv 3
rs397514474
TRPV4
0.925 0.120 12 109814565 missense variant C/A snv 3
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
rs369091875
DCHS1
0.925 0.240 11 6633485 missense variant C/G;T snv 1.1E-03 2
rs116571438
TRPV4
0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 2
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
rs267607147
TRPV4
0.925 0.120 12 109784379 missense variant G/A;C snv 2
rs267607150
TRPV4
0.925 0.080 12 109792671 missense variant T/C snv 2
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