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: rs11221322
rs11221322
5 0.827 0.120 11 128476898 intron variant T/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11221332
rs11221332
8 0.763 0.280 11 128511079 intron variant C/A;T snv 0.700 1.000 1 2016 2016