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: rs1646019
rs1646019
1 1.000 0.080 16 11265823 intron variant C/T snv 0.36 0.800 1.000 1 2012 2012
dbSNP: rs80073729
rs80073729
1 1.000 0.080 16 11279940 intron variant G/A snv 4.1E-03 0.700 1.000 1 2012 2012