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: rs119103214
rs119103214
1 1.000 0.120 3 183037218 missense variant C/G snv 0.700 0
dbSNP: rs119103215
rs119103215
1 1.000 0.120 3 183039093 missense variant A/G snv 0.700 0
dbSNP: rs119103216
rs119103216
1 1.000 0.120 3 183034068 missense variant G/A snv 0.700 0
dbSNP: rs119103218
rs119103218
1 1.000 0.120 3 183037432 missense variant A/C snv 0.700 0
dbSNP: rs1229069160
rs1229069160
1 1.000 0.120 3 183072457 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1311374961
rs1311374961
1 1.000 0.120 3 183092510 frameshift variant CT/- delins 4.0E-06 1.4E-05 0.700 0
dbSNP: rs1326114075
rs1326114075
1 1.000 0.120 3 183057318 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1333357031
rs1333357031
1 1.000 0.120 3 183041687 missense variant C/T snv 1.4E-05 0.700 0
dbSNP: rs150862707
rs150862707
1 1.000 0.120 3 183052169 stop gained A/G;T snv 4.1E-04; 1.2E-05 0.700 0
dbSNP: rs1553850609
rs1553850609
1 1.000 0.120 3 183022454 frameshift variant TTCGCTTTACTAGC/- delins 0.700 0
dbSNP: rs1553856095
rs1553856095
1 1.000 0.120 3 183045508 frameshift variant AT/- delins 0.700 0
dbSNP: rs1560224024
rs1560224024
1 1.000 0.120 3 183041571 frameshift variant GTACTCC/- delins 0.700 0
dbSNP: rs1560256569
rs1560256569
1 1.000 0.120 3 183071018 stop gained TCTC/GCTATGCTAT delins 0.700 0
dbSNP: rs185741664
rs185741664
1 1.000 0.120 3 183057343 stop gained G/A snv 4.5E-05 2.1E-05 0.700 0
dbSNP: rs199914879
rs199914879
1 1.000 0.120 3 183071208 splice donor variant A/T snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs398124350
rs398124350
1 1.000 0.120 3 183045422 frameshift variant C/- delins 0.700 0
dbSNP: rs727504004
rs727504004
1 1.000 0.120 3 183071066 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs748201122
rs748201122
1 1.000 0.120 3 183071310 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs750484977
rs750484977
1 1.000 0.120 3 183045516 stop gained G/C snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs754460336
rs754460336
1 1.000 0.120 3 183092486 missense variant G/A snv 6.4E-05 5.6E-05 0.700 0
dbSNP: rs757362635
rs757362635
1 1.000 0.120 3 183071290 missense variant A/G;T snv 2.4E-05; 1.2E-05 0.700 0
dbSNP: rs762463914
rs762463914
1 1.000 0.120 3 183099440 start lost T/C snv 1.8E-05 3.5E-05 0.700 0
dbSNP: rs773433541
rs773433541
1 1.000 0.120 3 183057358 missense variant A/C;G snv 8.1E-06 0.700 0
dbSNP: rs794727036
rs794727036
1 1.000 0.120 3 183041695 missense variant T/C;G snv 4.0E-06 0.700 0
dbSNP: rs796051985
rs796051985
1 1.000 0.120 3 183041640 frameshift variant CA/- delins 4.0E-06 1.4E-05 0.700 0