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: rs28934576
rs28934576
39 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs11540652
rs11540652
42 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
dbSNP: rs121912651
rs121912651
37 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs28934578
rs28934578
16 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs121913343
rs121913343
29 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 0.710 1.000 0 2011 2011
dbSNP: rs121912664
rs121912664
7 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 0.700 0
dbSNP: rs28934575
rs28934575
25 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 0
dbSNP: rs397516436
rs397516436
26 0.641 0.440 17 7674894 stop gained G/A;C snv 0.710 1.000 0 1998 1998
dbSNP: rs886039484
rs886039484
10 0.641 0.440 17 7674888 missense variant T/C;G snv 0.700 0
dbSNP: rs121912666
rs121912666
24 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.700 0
dbSNP: rs28934571
rs28934571
4 0.645 0.360 17 7674216 missense variant C/A;G snv 0.700 0
dbSNP: rs760043106
rs760043106
18 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 0
dbSNP: rs28934574
rs28934574
27 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs121912656
rs121912656
20 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs764146326
rs764146326
20 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 0.700 0
dbSNP: rs28934573
rs28934573
24 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs138729528
rs138729528
25 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 0.700 0
dbSNP: rs121912654
rs121912654
3 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 0.700 0
dbSNP: rs587780070
rs587780070
23 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs786201838
rs786201838
23 0.683 0.440 17 7674953 missense variant T/A;C;G snv 0.700 0
dbSNP: rs1057519981
rs1057519981
20 0.689 0.440 17 7674251 missense variant A/C;G;T snv 0.700 0
dbSNP: rs1057520002
rs1057520002
20 0.695 0.360 17 7674242 missense variant A/C;G snv 0.700 0
dbSNP: rs193920774
rs193920774
21 0.695 0.440 17 7673823 missense variant C/A;T snv 0.700 0
dbSNP: rs28934874
rs28934874
21 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 0
dbSNP: rs17849781
rs17849781
14 0.701 0.480 17 7673788 missense variant G/A;C;T snv 0.700 0