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: rs6441286
rs6441286
2 0.925 0.080 3 160011091 intron variant T/G snv 0.36 0.700 1.000 2 2009 2010
dbSNP: rs485499
rs485499
2 0.925 0.080 3 160028076 intron variant T/C snv 0.29 0.700 1.000 1 2011 2011