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: rs1351592
rs1351592
1 1.000 0.120 2 212529988 intron variant C/G snv 0.29 0.710 1.000 1 2015 2017
dbSNP: rs2178575
rs2178575
1 1.000 0.120 2 212527042 intron variant G/A;T snv 0.700 1.000 1 2018 2018