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: rs80356616
rs80356616
19 0.732 0.360 11 17387917 missense variant C/T snv 0.030 1.000 3 2006 2006
dbSNP: rs80356624
rs80356624
16 0.752 0.240 11 17387490 missense variant C/A;T snv 0.020 1.000 2 2005 2006
dbSNP: rs193929337
rs193929337
6 0.827 0.160 11 17387937 missense variant T/C snv 0.010 1.000 1 2014 2014
dbSNP: rs193929353
rs193929353
4 0.882 0.120 11 17387206 missense variant T/C;G snv 0.010 1.000 1 2005 2005
dbSNP: rs193929358
rs193929358
5 0.851 0.240 11 17387091 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs80356611
rs80356611
10 0.790 0.240 11 17387943 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs80356618
rs80356618
8 0.807 0.200 11 17387595 missense variant C/A;T snv 0.010 1.000 1 2006 2006