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: rs1411478
rs1411478
3 0.925 0.120 1 180993146 intron variant A/G snv 0.56 0.810 1.000 2 2011 2013
dbSNP: rs57113693
rs57113693
1 1.000 0.120 1 180983158 intron variant C/T snv 0.56 0.700 1.000 1 2018 2018