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: rs1554199368
rs1554199368
12 0.827 0.160 5 177256956 missense variant C/T snv 0.700 0
dbSNP: rs1554846212
rs1554846212
9 0.851 0.160 10 75030037 missense variant C/T snv 0.700 0
dbSNP: rs1556425596
rs1556425596
37 0.752 0.240 21 45989967 intron variant C/T snv 0.700 0
dbSNP: rs1557569831
rs1557569831
8 0.925 0.120 1 43431458 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1562134961
rs1562134961
13 0.776 0.320 6 78969879 frameshift variant A/- delins 0.700 0
dbSNP: rs1565295267
rs1565295267
6 0.827 0.360 11 61774051 missense variant C/A snv 0.700 0
dbSNP: rs1566823361
rs1566823361
18 0.742 0.440 13 101726732 frameshift variant -/G delins 0.700 0
dbSNP: rs180177135
rs180177135
27 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 0.700 0
dbSNP: rs200426926
rs200426926
13 0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 0.700 0
dbSNP: rs387906692
rs387906692
11 0.752 0.480 17 68530405 stop gained C/T snv 0.700 0
dbSNP: rs397507520
rs397507520
39 0.658 0.520 12 112453279 missense variant G/C;T snv 0.700 0
dbSNP: rs397507545
rs397507545
20 0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs397517154
rs397517154
16 0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs398122886
rs398122886
1 1.000 0.120 19 17817033 stop gained G/A snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs587784105
rs587784105
19 0.732 0.440 5 177235863 stop gained G/A snv 0.700 0
dbSNP: rs61729366
rs61729366
6 0.851 0.240 4 78511299 missense variant G/A snv 5.2E-03 5.8E-03 0.700 0
dbSNP: rs61752717
rs61752717
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.700 0
dbSNP: rs746200792
rs746200792
8 0.925 0.120 1 43437254 inframe deletion TGT/- delins 0.700 0
dbSNP: rs759317757
rs759317757
12 0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 0.700 0
dbSNP: rs765379963
rs765379963
19 0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs797045005
rs797045005
4 0.851 0.320 12 49185140 missense variant A/G snv 0.700 0
dbSNP: rs869312712
rs869312712
3 0.925 0.360 6 157084866 stop gained C/T snv 0.700 0
dbSNP: rs875989800
rs875989800
33 0.732 0.480 22 23833670 inframe deletion AGA/- delins 0.700 0
dbSNP: rs6523
rs6523
4 0.882 0.200 19 17821329 missense variant T/C snv 0.65 0.70 0.030 0.667 3 2000 2019
dbSNP: rs1110061
rs1110061
7 0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 0.020 1.000 2 2006 2015