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: rs2187668
rs2187668
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 1 2011 2011
dbSNP: rs9272729
rs9272729
1 1.000 0.120 6 32641817 intron variant G/A;C snv 0.710 1.000 1 2017 2017