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: rs8111874
rs8111874
1 19 48665685 intron variant G/A snv 0.32 0.710 1.000 1 2016 2016
dbSNP: rs12462111
rs12462111
2 19 48668049 intron variant C/T snv 0.33 0.700 1.000 1 2016 2016