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: rs12610645
rs12610645
1 19 2165843 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12982593
rs12982593
1 19 2175892 intron variant C/A snv 0.46 0.700 1.000 1 2017 2017