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
13 0.763 0.280 11 128511079 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1128334
rs1128334
5 0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs4937333
rs4937333
4 0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45 0.010 1.000 1 2014 2014