Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518663
ANKRD11
1.000 0.280 16 89283420 stop gained G/T snv 1
rs1057519399
ANKRD11
1.000 0.280 16 89281038 frameshift variant A/- del 2
rs1064793539
ANKRD11
1.000 0.280 16 89283458 stop gained G/T snv 1
rs1064794330
ANKRD11
1.000 0.280 16 89283315 frameshift variant CTTT/- delins 1
rs1114167291
ANKRD11
0.790 0.280 16 89281225 stop gained C/A snv 10
rs1135401804
ANKRD11
1.000 0.280 16 89283895 stop gained C/A snv 1
rs1135401815
ANKRD11
1.000 0.280 16 89279755 frameshift variant -/T ins 1
rs1221781038
ANKRD11
0.925 0.280 16 89279695 stop gained G/A;T snv 2
rs1381957912
ANKRD11
1.000 0.280 16 89279872 stop gained C/A;T snv 5.5E-06 1
rs1555521799
ANKRD11
1.000 0.280 16 89270872 missense variant G/T snv 2
rs1555524861
ANKRD11
1.000 16 89279215 stop gained G/A snv 1
rs1555525115
ANKRD11
0.851 0.360 16 89279567 frameshift variant GGCTTCGG/- delins 5
rs1555525977
ANKRD11
1.000 0.280 16 89280344 stop gained GA/TT mnv 1
rs1555526796
ANKRD11
1.000 16 89281005 frameshift variant A/- delins 1
rs1555527341
ANKRD11
1.000 0.280 16 89281489 frameshift variant T/- del 1
rs1555527497
ANKRD11
1.000 16 89281640 frameshift variant A/- del 1
rs1555527929
ANKRD11
1.000 0.280 16 89282254 stop gained T/A snv 1
rs1555528356
ANKRD11
0.790 0.360 16 89282836 stop gained G/A snv 13
rs1555528357
ANKRD11
1.000 16 89282837 frameshift variant ATTT/- delins 2
rs1555528400
ANKRD11
1.000 0.280 16 89282909 frameshift variant TT/- delins 1
rs1555528558
ANKRD11
1.000 16 89283207 frameshift variant -/T delins 3
rs1555529052
ANKRD11
1.000 16 89284048 frameshift variant T/- del 1
rs1555529181
ANKRD11
1.000 0.280 16 89284135 frameshift variant GAGT/- delins 1
rs1555529297
ANKRD11
1.000 16 89284412 stop gained C/T snv 2
rs1555529551
ANKRD11
1.000 0.280 16 89284863 stop gained G/C snv 1