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: rs485499
rs485499
2 0.925 0.080 3 160028076 intron variant T/C snv 0.29 0.800 1.000 3 2011 2015
dbSNP: rs2366643
rs2366643
1 1.000 0.080 3 160018698 intron variant T/C;G snv 0.800 1.000 1 2012 2012