Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137854521
rs137854521
9 0.851 0.200 11 22221100 frameshift variant -/A delins 0.700 0
dbSNP: rs1057518952
rs1057518952
3 1.000 0.080 6 52024728 frameshift variant -/C delins 0.700 0
dbSNP: rs1555452653
rs1555452653
1 16 2105909 frameshift variant -/C delins 0.700 0
dbSNP: rs1555450475
rs1555450475
2 1.000 0.120 16 2102583 frameshift variant -/G delins 0.700 0
dbSNP: rs886039793
rs886039793
4 0.882 0.120 19 45227667 frameshift variant -/G delins 0.700 0
dbSNP: rs1567202189
rs1567202189
2 1.000 0.080 16 2111276 inframe insertion -/GTG ins 0.700 0
dbSNP: rs1555448106
rs1555448106
2 1.000 0.120 16 2097160 frameshift variant A/- del 0.700 0
dbSNP: rs1555454915
rs1555454915
2 1.000 0.120 16 2109358 frameshift variant A/- del 0.700 0
dbSNP: rs1556009247
rs1556009247
7 0.882 X 72490973 missense variant A/C;T snv 0.700 0
dbSNP: rs1057518959
rs1057518959
2 16 2091794 missense variant A/G snv 0.700 0
dbSNP: rs1555459345
rs1555459345
3 1.000 0.040 16 2119114 missense variant A/G snv 0.700 0
dbSNP: rs886039804
rs886039804
4 0.882 0.120 11 61366050 missense variant A/G snv 0.700 0
dbSNP: rs786205134
rs786205134
3 0.925 0.160 11 111840653 splice donor variant A/T snv 0.700 1.000 1 2016 2016
dbSNP: rs886039803
rs886039803
3 0.925 0.120 17 58216664 splice donor variant A/T snv 0.700 0
dbSNP: rs886039805
rs886039805
5 0.925 0.120 12 88129872 frameshift variant AA/- delins 0.700 0
dbSNP: rs770908659
rs770908659
2 1.000 0.120 20 10412556 frameshift variant AG/- delins 8.0E-06 7.0E-06 0.700 0
dbSNP: rs886040959
rs886040959
2 1.000 0.120 16 2090962 frameshift variant AGTGAAGCGGCGCGGGCGGCCGCGCA/TCACTAGCTT delins 0.700 0
dbSNP: rs886039791
rs886039791
5 0.882 0.160 5 134893572 inframe deletion AGTTTGGCCCCTCAC/- delins 0.700 0
dbSNP: rs1555452400
rs1555452400
2 1.000 0.120 16 2105412 frameshift variant AT/- delins 0.700 0
dbSNP: rs1555446033
rs1555446033
2 1.000 0.120 16 2092144 frameshift variant C/- delins 0.700 0
dbSNP: rs886039813
rs886039813
8 0.827 0.160 X 13756600 frameshift variant C/- delins 0.700 0
dbSNP: rs566014072
rs566014072
3 16 2110321 stop gained C/A;G;T snv 8.0E-06; 8.0E-06 0.700 0
dbSNP: rs780009030
rs780009030
2 1.000 0.120 16 2097376 stop gained C/A;T snv 4.1E-06 1.4E-05 0.700 0
dbSNP: rs1458766475
rs1458766475
41 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2020 2020
dbSNP: rs1057518906
rs1057518906
1 4 88007878 stop gained C/T snv 1.4E-05 0.700 0