Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs66527965
COL1A1
0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs869312694
MAGEL2
0.925 0.120 15 23644535 stop gained C/A snv 3
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
rs121912633
TRPV4
0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs77975504
TRPV4
0.827 0.280 12 109792695 missense variant C/T snv 6
rs121912637
TRPV4
0.851 0.160 12 109784378 missense variant G/A;C snv 5
rs267607149
TRPV4
0.851 0.120 12 109784385 missense variant C/T snv 5
rs387906904
TRPV4
0.851 0.080 12 109803009 missense variant G/A snv 5
rs267607148
TRPV4
0.882 0.120 12 109800639 missense variant C/T snv 4
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
rs886044555
COL2A1
0.925 0.080 12 47985772 missense variant C/T snv 3
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