Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555528356
ANKRD11
0.790 0.360 16 89282836 stop gained G/A snv 13
rs1114167291
ANKRD11
0.790 0.280 16 89281225 stop gained C/A snv 10
rs869312713
ANKRD11
0.882 0.320 16 89280070 stop gained C/A snv 6
rs1555529297
ANKRD11
1.000 16 89284412 stop gained C/T snv 2
rs1221781038
ANKRD11
0.925 0.280 16 89279695 stop gained G/A;T snv 2
rs763407068
ANKRD11
1.000 0.280 16 89280330 stop gained G/A;C snv 5.6E-05 2
rs886041791
ANKRD11
0.925 0.280 16 89284345 stop gained G/A;T snv 2
rs1567574466
ANKRD11
1.000 0.040 16 89283404 stop gained A/T snv 1
rs1064793539
ANKRD11
1.000 0.280 16 89283458 stop gained G/T snv 1
rs1135401804
ANKRD11
1.000 0.280 16 89283895 stop gained C/A snv 1
rs1555525977
ANKRD11
1.000 0.280 16 89280344 stop gained GA/TT mnv 1
rs1381957912
ANKRD11
1.000 0.280 16 89279872 stop gained C/A;T snv 5.5E-06 1
rs749201074
ANKRD11
1.000 0.280 16 89284565 stop gained G/A;C snv 1.2E-05 7.0E-06 1
rs761636251
ANKRD11
1.000 0.280 16 89286064 stop gained G/A;T snv 8.0E-06 1
rs1057518663
ANKRD11
1.000 0.280 16 89283420 stop gained G/T snv 1
rs1555529551
ANKRD11
1.000 0.280 16 89284863 stop gained G/C snv 1
rs1555527929
ANKRD11
1.000 0.280 16 89282254 stop gained T/A snv 1
rs863225296
ANKRD11
1.000 0.280 16 89279362 stop gained G/A snv 1
rs761848111
ANKRD11
1.000 0.280 16 89282980 stop gained G/A snv 1
rs749632782
ANKRD11
1.000 0.280 16 89282336 stop gained G/A;C snv 2.0E-05 7.0E-06 1
rs1567579525
ANKRD11
1.000 0.280 16 89284594 stop gained G/A snv 1
rs1555524861
ANKRD11
1.000 16 89279215 stop gained G/A snv 1
rs1555521799
ANKRD11
1.000 0.280 16 89270872 missense variant G/T snv 2
rs797044890
ANKRD11
16 89275092 splice donor variant C/T snv 1
rs879253753
ANKRD11
0.851 0.280 16 89280526 frameshift variant -/T delins 19