Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543120965
CLCN1
0.925 0.120 7 143332409 intron variant T/C snv 1.2E-05 3.5E-05 2
rs55960271
CLCN1
0.882 0.120 7 143351678 stop gained C/A;T snv 4.0E-06; 2.9E-03 5
rs1057518917
CLCN1
0.925 0.120 7 143351633 stop gained C/T snv 8.0E-06 1.4E-05 3
rs1554436419
CLCN1
0.925 0.120 7 143330816 stop gained CG/TA mnv 2
rs1554436799
CLCN1
0.925 0.120 7 143332431 stop gained T/A snv 2
rs201714423
CLCN1
0.925 0.120 7 143331615 stop gained C/T snv 1.2E-05 1.4E-05 2
rs201894078
CLCN1
0.925 0.120 7 143342451 stop gained C/T snv 1.4E-05 2
rs369773321
CLCN1
0.925 0.120 7 143321720 stop gained G/A;T snv 1.6E-05; 4.4E-05 2
rs759761559
CLCN1
0.925 0.120 7 143331264 stop gained C/T snv 2
rs1554434400
CLCN1
1.000 0.120 7 143319794 stop gained C/T snv 1
rs1554439817
CLCN1
1.000 0.120 7 143350387 stop gained C/T snv 1
rs797045032
CLCN1
0.827 0.280 7 143321720 missense variant GG/TC mnv 11
rs80356702
CLCN1
0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
rs149729531
CLCN1
0.851 0.200 7 143321432 missense variant C/G snv 1.2E-03 7.5E-04 6
rs80356704
CLCN1
0.827 0.200 7 143341938 missense variant C/T snv 4.4E-05 2.1E-05 6
rs80356690
CLCN1
0.882 0.120 7 143330788 missense variant C/G;T snv 1.2E-05 4
rs80356696
CLCN1
0.851 0.120 7 143342001 missense variant A/G;T snv 4
rs121912799
CLCN1
0.882 0.120 7 143332490 missense variant T/G snv 3.7E-04 2.7E-04 3
rs146457619
CLCN1
0.882 0.120 7 143339304 missense variant A/G snv 4.0E-04 3.8E-04 3
rs748537564
CLCN1
0.882 0.160 7 143345595 missense variant C/A;T snv 9.5E-05 3
rs757109632
CLCN1
0.882 0.120 7 143324468 missense variant T/C snv 2.1E-05 3
rs762754992
CLCN1
0.882 0.120 7 143341995 missense variant C/T snv 1.6E-05 3
rs764100025
CLCN1
0.882 0.120 7 143330810 missense variant G/A snv 1.6E-05 3
rs80356687
CLCN1
0.882 0.120 7 143324442 missense variant C/T snv 1.2E-05 2.1E-05 3
rs80356692
CLCN1
0.882 0.120 7 143330855 missense variant G/A snv 4.0E-06 1.4E-05 3