Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1557570794
rs1557570794
0.742 0.120 1 26697152 frameshift variant -/GCCGCCTCCCTCCTCCAGCGCC delins
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1557781252
rs1557781252
0.742 0.320 1 153816414 stop gained G/A snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1558373252
rs1558373252
0.790 0.120 2 5693013 frameshift variant T/- delins
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1559470315
rs1559470315
0.732 0.320 3 41227287 protein altering variant CCACAAGCAG/T delins
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1561964103
rs1561964103
0.882 0.080 6 50836108 frameshift variant G/- delins
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1564919048
rs1564919048
0.732 0.280 10 121520106 missense variant C/A snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1567941252
rs1567941252
0.807 0.240 17 38739601 missense variant G/A snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1569301036
rs1569301036
0.827 0.240 X 71397354 missense variant C/T snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs1569509136
rs1569509136
0.708 0.400 X 53647576 splice acceptor variant T/C snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs190521996
rs190521996
0.790 0.320 16 8811660 missense variant T/C snv 2.9E-04 4.1E-04
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs199476133
rs199476133
ATP6 ; ATP8 ; COX3 ; ND3 ; ND4 ; ND4L
0.742 0.320 MT 8993 missense variant T/C;G snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs28934907
rs28934907
0.732 0.320 X 154032268 missense variant G/A;C snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs397507539
rs397507539
0.851 0.160 12 112489047 missense variant C/A;G;T snv 4.0E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs397507540
rs397507540
0.851 0.160 12 112489048 missense variant C/A;T snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs397507547
rs397507547
0.752 0.280 12 112489086 missense variant A/G snv 4.0E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs398124401
rs398124401
0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs559979281
rs559979281
0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs587784347
rs587784347
0.742 0.280 22 38113561 missense variant G/A snv 8.0E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs753317536
rs753317536
EVC
0.790 0.160 4 5719239 intron variant G/A;C snv 8.0E-06; 4.0E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs776720232
rs776720232
0.827 0.240 17 39673099 missense variant T/C;G snv 4.2E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs794727931
rs794727931
0.790 0.240 11 78112692 missense variant A/C snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs80338701
rs80338701
0.776 0.360 16 8811088 stop gained C/A;T snv 4.4E-05; 5.4E-06
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs80338945
rs80338945
0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs863225422
rs863225422
0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0
dbSNP: rs886039792
rs886039792
0.807 0.280 5 134874531 splice donor variant G/A snv
CUI: C0239234
Disease: Low set ears
Low set ears
0.700 0