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: rs1057516037
rs1057516037
4 0.925 X 72464626 protein altering variant TGGAG/AC delins 0.700 1.000 1 2016 2016
dbSNP: rs1057516038
rs1057516038
5 0.925 14 58444158 stop gained C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057517846
rs1057517846
2 1.000 16 78108446 stop gained G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs1310897090
rs1310897090
2 1.000 2 15467394 stop gained G/A snv 0.010 1.000 1 2017 2017
dbSNP: rs1447313633
rs1447313633
4 1.000 2 218649090 frameshift variant TT/- del 0.700 1.000 1 2019 2019
dbSNP: rs145536528
rs145536528
3 1.000 5 160413521 missense variant G/A snv 1.6E-05 3.5E-05 0.010 1.000 1 2016 2016
dbSNP: rs1554817910
rs1554817910
4 1.000 10 79216266 missense variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs1559296368
rs1559296368
4 1.000 2 218646330 frameshift variant C/- del 0.700 1.000 1 2019 2019
dbSNP: rs398123001
rs398123001
4 0.925 8 143818378 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs574384755
rs574384755
1 1.000 20 63490507 missense variant G/A snv 4.1E-06 0.010 1.000 1 2017 2017
dbSNP: rs587777585
rs587777585
6 0.882 6 30918851 missense variant C/G;T snv 2.4E-05 0.010 1.000 1 2019 2019
dbSNP: rs757533393
rs757533393
2 1.000 20 32216664 missense variant C/G;T snv 1.2E-05 0.010 1.000 1 2018 2018
dbSNP: rs758432471
rs758432471
4 0.925 1 1806513 missense variant C/T snv 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs786203986
rs786203986
3 0.925 13 101176371 missense variant G/A;C snv 4.3E-06 0.010 1.000 1 2016 2016
dbSNP: rs797044519
rs797044519
9 0.925 21 37478285 stop gained C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs797044520
rs797044520
6 0.925 21 37505442 stop gained C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs797044521
rs797044521
8 0.925 21 37480768 frameshift variant A/- delins 0.700 1.000 1 2015 2015
dbSNP: rs797044522
rs797044522
9 0.925 21 37496119 frameshift variant AGAT/- delins 0.700 1.000 1 2015 2015
dbSNP: rs797044523
rs797044523
9 0.882 21 37480756 frameshift variant -/A delins 0.700 1.000 1 2015 2015
dbSNP: rs797044524
rs797044524
9 0.925 21 37486513 missense variant A/T snv 0.700 1.000 1 2015 2015
dbSNP: rs797044525
rs797044525
9 0.925 21 37490244 missense variant T/G snv 0.700 1.000 1 2015 2015
dbSNP: rs797044526
rs797044526
7 0.925 21 37490393 missense variant C/T snv 0.700 1.000 1 2015 2015
dbSNP: rs1057518770
rs1057518770
6 1.000 15 25354536 missense variant C/T snv 0.700 0
dbSNP: rs1057518786
rs1057518786
5 1.000 6 33441374 splice region variant G/A snv 0.700 0
dbSNP: rs1057518796
rs1057518796
3 1.000 6 33443751 frameshift variant C/- delins 0.700 0