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: rs209473
rs209473
1 1.000 0.120 6 32955131 intron variant A/C snv 0.56 0.700 1.000 1 2007 2007
dbSNP: rs580962
rs580962
1 1.000 0.120 6 32957915 intron variant C/T snv 0.64 0.700 1.000 1 2007 2007