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: rs7255436
rs7255436
2 19 8368312 intron variant C/A snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs2278236
rs2278236
2 19 8366697 intron variant G/A;C snv 0.700 1.000 1 2012 2012