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 4 2008 2016
dbSNP: rs9273076
rs9273076
1 1.000 0.080 6 32644524 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2015 2015