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: rs177430
rs177430
4 18 23506161 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1808579
rs1808579
3 18 23524924 intron variant C/T snv 0.47 0.700 1.000 1 2015 2015