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: rs28934575
rs28934575
37 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.810 1.000 52 1990 2017
dbSNP: rs121912664
rs121912664
44 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 0.900 0.977 44 1990 2020
dbSNP: rs121912666
rs121912666
34 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.820 1.000 43 1990 2018
dbSNP: rs28934576
rs28934576
78 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.820 1.000 38 1990 2018
dbSNP: rs587782144
rs587782144
8 0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.810 1.000 37 1990 2017
dbSNP: rs121912651
rs121912651
53 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.820 1.000 34 1990 2015
dbSNP: rs587782705
rs587782705
8 0.807 0.280 17 7675157 missense variant G/A snv 8.0E-06 0.800 1.000 34 1990 2017
dbSNP: rs138729528
rs138729528
25 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 0.800 1.000 29 1990 2015
dbSNP: rs28934578
rs28934578
47 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.820 1.000 28 1990 2017
dbSNP: rs587780070
rs587780070
24 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 0.800 1.000 27 1990 2017
dbSNP: rs587782596
rs587782596
7 0.807 0.200 17 7675071 missense variant G/A;T snv 0.800 1.000 27 1990 2017
dbSNP: rs28934574
rs28934574
31 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.800 1.000 26 1990 2017
dbSNP: rs397514495
rs397514495
4 0.882 0.120 17 7675070 missense variant C/A;T snv 1.2E-05 0.800 1.000 26 1990 2016
dbSNP: rs879253942
rs879253942
28 0.677 0.400 17 7673826 missense variant A/G snv 0.800 1.000 25 1990 2017
dbSNP: rs587778720
rs587778720
31 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 0.810 1.000 24 1990 2015
dbSNP: rs121913343
rs121913343
44 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 0.800 1.000 23 1988 2014
dbSNP: rs121912656
rs121912656
28 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.800 1.000 22 1990 2014
dbSNP: rs587782529
rs587782529
8 0.851 0.200 17 7670700 missense variant G/A;C snv 0.810 1.000 22 1990 2014
dbSNP: rs121912662
rs121912662
2 0.925 0.120 17 7670678 missense variant A/G snv 0.800 1.000 21 1990 2017
dbSNP: rs587781288
rs587781288
16 0.732 0.440 17 7675190 missense variant C/A;T snv 0.800 1.000 20 1990 2014
dbSNP: rs786201838
rs786201838
24 0.683 0.440 17 7674953 missense variant T/A;C;G snv 0.800 1.000 20 1990 2017
dbSNP: rs876660754
rs876660754
20 0.701 0.360 17 7675095 missense variant C/A;T snv 0.800 1.000 20 1990 2018
dbSNP: rs121912663
rs121912663
2 0.925 0.120 17 7673745 missense variant T/A;C snv 0.710 1.000 19 1990 2017
dbSNP: rs28934874
rs28934874
21 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.800 1.000 19 1990 2014
dbSNP: rs730882005
rs730882005
20 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 0.800 1.000 19 1994 2016