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: rs587779388
rs587779388
1.000 1 113898755 frameshift variant GT/- delins 1.4E-04 1.5E-04
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 3 2011 2012
dbSNP: rs1057524157
rs1057524157
0.776 0.200 11 686962 missense variant A/C;T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 2 2017 2017
dbSNP: rs1057519565
rs1057519565
0.851 0.200 11 687941 missense variant C/T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 1 2017 2017
dbSNP: rs1554333853
rs1554333853
0.689 0.320 7 40046006 missense variant A/G snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 1 2017 2017
dbSNP: rs1554817910
rs1554817910
1.000 10 79216266 missense variant A/G snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 1 2019 2019
dbSNP: rs1555743003
rs1555743003
0.701 0.520 18 33740444 splice donor variant G/A snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 1.000 1 2016 2016
dbSNP: rs1009298200
rs1009298200
0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1057518796
rs1057518796
1.000 6 33443751 frameshift variant C/- delins
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1057518848
rs1057518848
0.827 0.240 18 55229003 frameshift variant -/ATTG delins
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1057518921
rs1057518921
1.000 X 71132465 missense variant G/A snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1057519389
rs1057519389
0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1057524820
rs1057524820
0.776 0.280 12 51765746 missense variant G/A;T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1064795760
rs1064795760
0.882 0.080 9 92719007 inframe deletion ATT/- del
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1064797102
rs1064797102
0.827 0.120 8 91071136 splice acceptor variant A/G snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1131692228
rs1131692228
0.925 0.160 7 100646637 missense variant C/T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1131692231
rs1131692231
0.827 0.280 5 157294834 missense variant C/T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs114925667
rs114925667
0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1325394060
rs1325394060
0.851 0.320 X 53534144 missense variant C/G;T snv 9.5E-06
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs142239530
rs142239530
0.790 0.320 11 4091328 missense variant C/G;T snv 4.4E-05
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1553212868
rs1553212868
0.807 0.280 1 151406264 frameshift variant G/- delins
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1553511224
rs1553511224
0.882 0.080 2 161423825 frameshift variant -/C delins
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1553621496
rs1553621496
0.677 0.440 2 209976305 splice donor variant T/G snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0
dbSNP: rs1553632357
rs1553632357
0.882 0.120 3 41236421 stop gained G/T snv
CUI: C1854882
Disease: Absent speech
Absent speech
0.700 0