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: rs1519480
rs1519480
4 0.925 0.040 11 27654165 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs1565228
rs1565228
4 11 27564889 intron variant G/A;C snv 0.700 1.000 1 2018 2018