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: rs1614972
rs1614972
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.010 1.000 1 2014 2014
dbSNP: rs1789903
rs1789903
1 1.000 0.080 4 99340884 intron variant C/A;G snv 0.010 1.000 1 2014 2014
dbSNP: rs1789924
rs1789924
5 0.925 0.160 4 99353129 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013