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: rs2569190
rs2569190
39 0.620 0.560 5 140633331 intron variant A/G snv 0.57 0.010 1.000 1 2011 2011
dbSNP: rs5744441
rs5744441
1 1.000 0.080 5 140637262 upstream gene variant G/A;C snv 0.010 1.000 1 2011 2011