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: rs863225264
rs863225264
6 0.827 0.240 1 11130747 missense variant C/T snv 0.810 1.000 1 2017 2017
dbSNP: rs869312666
rs869312666
4 0.925 0.160 1 11129789 missense variant A/C snv 0.800 1.000 3 2015 2016
dbSNP: rs878855328
rs878855328
4 0.882 0.120 1 11117039 missense variant C/T snv 0.800 1.000 3 2015 2016
dbSNP: rs869312671
rs869312671
5 0.882 0.160 1 11144735 missense variant C/T snv 0.800 0
dbSNP: rs369088781
rs369088781
1 1.000 1 11130648 missense variant C/A;T snv 8.1E-06; 1.6E-05 0.700 1.000 3 2015 2016
dbSNP: rs1057519915
rs1057519915
5 0.851 0.160 1 11109318 missense variant A/C snv 0.700 0
dbSNP: rs786205165
rs786205165
4 0.882 0.120 1 11157173 missense variant C/A;T snv 0.700 0