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 0.020 1.000 2 2011 2012
dbSNP: rs2915863
rs2915863
3 0.925 0.160 5 140634792 upstream gene variant C/A;T snv 0.010 1.000 1 2014 2014