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: rs724159949
rs724159949
15 0.827 0.240 21 37486563 stop gained C/T snv 0.700 1.000 1 2015 2015
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: rs1057519402
rs1057519402
2 1.000 21 37478266 frameshift variant CTTGA/- delins 0.700 0
dbSNP: rs724159948
rs724159948
7 1.000 21 37490273 stop gained C/T snv 0.700 0
dbSNP: rs724159950
rs724159950
6 1.000 0.200 21 37486571 frameshift variant TGAG/GAA delins 0.700 0
dbSNP: rs724159951
rs724159951
6 21 37493101 missense variant T/C snv 0.700 0
dbSNP: rs724159952
rs724159952
6 21 37490451 frameshift variant -/G delins 0.700 0
dbSNP: rs724159953
rs724159953
7 1.000 21 37505352 stop gained C/T snv 0.700 0
dbSNP: rs724159954
rs724159954
6 21 37490353 frameshift variant -/A delins 0.700 0
dbSNP: rs724159955
rs724159955
6 1.000 21 37512002 missense variant C/A snv 0.700 0
dbSNP: rs724159956
rs724159956
6 21 37496249 frameshift variant -/G delins 0.700 0