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: rs1470145133
rs1470145133
1 1.000 20 63693183 missense variant T/G snv 4.0E-06 0.700 1.000 5 2013 2013
dbSNP: rs398123016
rs398123016
1 1.000 20 63690161 missense variant G/T snv 0.700 1.000 5 2013 2013
dbSNP: rs398123019
rs398123019
1 1.000 20 63672607 missense variant G/A snv 0.700 1.000 5 2013 2013
dbSNP: rs1161373315
rs1161373315
1 1.000 20 63662876 stop gained C/A;T snv 7.0E-06 0.700 0
dbSNP: rs1263776141
rs1263776141
1 1.000 20 63689639 frameshift variant -/G delins 7.0E-06 0.700 0
dbSNP: rs1415449695
rs1415449695
1 1.000 20 63694761 stop gained C/G;T snv 7.0E-06 0.700 0
dbSNP: rs1421904176
rs1421904176
1 1.000 20 63693004 splice donor variant G/T snv 4.0E-06 0.700 0
dbSNP: rs1555811386
rs1555811386
1 1.000 20 63688138 splice acceptor variant G/A snv 0.700 0
dbSNP: rs1555811742
rs1555811742
1 1.000 20 63689581 frameshift variant -/C delins 0.700 0
dbSNP: rs1555811966
rs1555811966
1 1.000 20 63690212 splice donor variant T/A snv 0.700 0
dbSNP: rs1555812178
rs1555812178
1 1.000 20 63690803 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1555812228
rs1555812228
1 1.000 20 63690922 frameshift variant G/- delins 0.700 0
dbSNP: rs1555812480
rs1555812480
1 1.000 20 63691819 frameshift variant C/- delins 0.700 0
dbSNP: rs1555812834
rs1555812834
1 1.000 20 63692803 splice acceptor variant A/C snv 0.700 0
dbSNP: rs1555813123
rs1555813123
1 1.000 20 63693149 frameshift variant A/- del 0.700 0
dbSNP: rs1555813144
rs1555813144
1 1.000 20 63693172 stop gained A/T snv 0.700 0
dbSNP: rs1555814044
rs1555814044
1 1.000 20 63694478 frameshift variant -/C delins 0.700 0
dbSNP: rs1555814334
rs1555814334
1 1.000 20 63694961 frameshift variant C/- delins 0.700 0
dbSNP: rs1555899932
rs1555899932
2 0.925 20 63662886 stop gained G/T snv 0.700 0
dbSNP: rs1555901000
rs1555901000
1 1.000 20 63667484 stop gained C/A snv 0.700 0
dbSNP: rs1555901832
rs1555901832
1 1.000 20 63674071 frameshift variant C/- del 0.700 0
dbSNP: rs377024903
rs377024903
1 1.000 20 63690205 stop gained C/G;T snv 4.0E-06 0.700 0
dbSNP: rs377461417
rs377461417
1 1.000 20 63694739 splice acceptor variant A/C;T snv 1.7E-05; 4.2E-06 0.700 0
dbSNP: rs398123048
rs398123048
1 1.000 20 63689821 missense variant C/G snv 0.700 0
dbSNP: rs398123049
rs398123049
1 1.000 20 63690178 missense variant G/A snv 0.700 0