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: rs2746071
rs2746071
4 0.882 0.160 1 192808434 intron variant A/G snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs1800764
rs1800764
10 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs4459609
rs4459609
4 0.925 0.120 17 63471587 upstream gene variant C/A snv 0.63 0.010 1.000 1 2014 2014