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: rs12809354
rs12809354
1 1.000 0.080 12 32825503 intron variant T/C snv 0.14 0.700 1.000 2 2018 2018
dbSNP: rs1454934
rs1454934
1 1.000 0.080 12 32820006 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017