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: rs16861329
rs16861329
1 0.882 0.160 3 186948673 intron variant C/T snv 0.13 0.800 1.000 2 2011 2013
dbSNP: rs3887925
rs3887925
1 1.000 0.080 3 186947857 intron variant C/T snv 0.43 0.700 1.000 3 2018 2019