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: rs149617956
rs149617956
32 0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 0.700 1.000 4 2011 2016
dbSNP: rs1060505041
rs1060505041
34 0.716 0.400 19 13136099 missense variant C/A;T snv 0.700 0
dbSNP: rs1135401778
rs1135401778
20 0.752 0.400 17 67854315 frameshift variant T/- del 0.700 1.000 1 2017 2017
dbSNP: rs1043679457
rs1043679457
33 0.752 0.400 5 60927745 intron variant C/A;G;T snv 0.700 0
dbSNP: rs267607048
rs267607048
16 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 0.700 0
dbSNP: rs144078282
rs144078282
9 0.776 0.400 11 72302339 missense variant T/A;C snv 1.8E-04; 2.0E-04 0.700 0
dbSNP: rs1553920379
rs1553920379
27 0.776 0.160 4 101032294 frameshift variant -/AGTA delins 0.700 0
dbSNP: rs200203460
rs200203460
9 0.776 0.400 11 72302312 stop gained G/A;C;T snv 2.8E-05 0.700 0
dbSNP: rs797045412
rs797045412
17 0.776 0.280 9 92718565 missense variant G/A;T snv 0.700 0
dbSNP: rs1564341846
rs1564341846
8 0.790 0.280 9 131508926 missense variant C/A snv 0.700 0
dbSNP: rs1553154130
rs1553154130
18 0.807 0.280 1 8358231 missense variant T/A;C snv 0.700 0
dbSNP: rs1567815105
rs1567815105
7 0.807 0.240 16 57660794 frameshift variant -/T delins 0.700 0
dbSNP: rs72555360
rs72555360
8 0.807 0.280 3 33058221 missense variant G/A snv 4.4E-05 6.3E-05 0.700 0
dbSNP: rs796052676
rs796052676
10 0.807 0.200 8 132180246 missense variant G/A snv 0.700 0
dbSNP: rs886039903
rs886039903
6 0.807 0.200 3 192335434 missense variant C/T snv 0.700 0
dbSNP: rs797045140
rs797045140
6 0.827 0.200 X 53238308 splice region variant TG/- delins 0.700 1.000 1 2016 2016
dbSNP: rs1135402761
rs1135402761
11 0.827 0.320 12 79448958 missense variant T/C snv 0.700 0
dbSNP: rs1559759089
rs1559759089
14 0.827 0.200 3 113795101 missense variant C/A snv 0.700 0
dbSNP: rs1568359734
rs1568359734
8 0.827 0.240 18 33738903 frameshift variant A/- delins 0.700 0
dbSNP: rs371582179
rs371582179
7 0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05 0.700 0
dbSNP: rs56144125
rs56144125
6 0.827 0.240 11 6617154 splice acceptor variant C/A;G;T snv 4.0E-04; 1.2E-05 0.700 0
dbSNP: rs863225082
rs863225082
7 0.827 0.160 6 43007265 missense variant G/A snv 0.700 0
dbSNP: rs869312702
rs869312702
10 0.827 0.160 9 128203609 missense variant G/A snv 0.700 0
dbSNP: rs886041093
rs886041093
7 0.827 0.280 9 137815998 missense variant G/A snv 0.700 0
dbSNP: rs886041095
rs886041095
11 0.827 0.160 12 13571930 missense variant C/T snv 0.700 0