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: rs121913468
rs121913468
7 0.827 0.160 17 39724008 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs121913474
rs121913474
9 0.790 0.200 10 121515260 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs138729528
rs138729528
25 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 0.700 1.000 1 2016 2016
dbSNP: rs148924904
rs148924904
17 0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs149680468
rs149680468
15 0.742 0.320 4 152326137 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs17849781
rs17849781
22 0.701 0.480 17 7673788 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs193920774
rs193920774
22 0.695 0.440 17 7673823 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs28934573
rs28934573
28 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs28934574
rs28934574
31 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs28934575
rs28934575
37 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs28934576
rs28934576
78 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.700 1.000 1 2016 2016
dbSNP: rs28934874
rs28934874
21 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs375874539
rs375874539
15 0.732 0.320 17 7674237 missense variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs377767347
rs377767347
14 0.742 0.520 18 51065549 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs387906678
rs387906678
5 0.851 0.120 10 121515263 missense variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs397516436
rs397516436
34 0.641 0.440 17 7674894 stop gained G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs483352697
rs483352697
21 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587778720
rs587778720
31 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587780070
rs587780070
24 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587780073
rs587780073
19 0.708 0.400 17 7674262 missense variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs587781991
rs587781991
17 0.724 0.240 17 7675208 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587782177
rs587782177
11 0.763 0.200 17 7674887 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587782329
rs587782329
23 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs587782664
rs587782664
15 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs730882005
rs730882005
20 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 1 2016 2016