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: rs12908437
rs12908437
5 0.882 0.200 15 98744146 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs28657002
rs28657002
1 15 98726649 intron variant T/A;C snv 0.700 1.000 1 2018 2018