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: rs2249742
rs2249742
7 0.925 0.120 6 31272944 intron variant C/T snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs2395471
rs2395471
5 0.925 0.120 6 31272915 intron variant G/A snv 0.47 0.700 1.000 1 2007 2007