Source: CURATED ×
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: rs121912656
rs121912656
20 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.710 1.000 1 2012 2016
dbSNP: rs121912660
rs121912660
18 0.683 0.240 17 7673781 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs121912666
rs121912666
24 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.710 1.000 1 2016 2019
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: rs193920774
rs193920774
21 0.695 0.440 17 7673823 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs28934574
rs28934574
27 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
25 0.641 0.400 17 7674230 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
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 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
11 0.732 0.320 17 7674237 missense variant G/A;C snv 0.710 0.500 1 2009 2016
dbSNP: rs397516436
rs397516436
26 0.641 0.440 17 7674894 stop gained G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs530941076
rs530941076
20 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587778720
rs587778720
25 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
23 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs587780071
rs587780071
11 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs587780073
rs587780073
17 0.708 0.400 17 7674262 missense variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs587781525
rs587781525
21 0.689 0.480 17 7673778 missense variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs587781991
rs587781991
14 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
16 0.677 0.280 17 7674217 missense variant C/A;G;T snv 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
dbSNP: rs730882008
rs730882008
22 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs753660142
rs753660142
19 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 0.700 1.000 1 2016 2016
dbSNP: rs760043106
rs760043106
18 0.645 0.440 17 7674947 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016