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: rs12016871
rs12016871
2 13 27443645 intron variant C/T snv 0.700 1.000 3 2015 2017
dbSNP: rs1218822
rs1218822
1 13 27437826 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4771122
rs4771122
4 1.000 0.080 13 27446043 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs9581854
rs9581854
1 13 27443645 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018