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: rs12930834
rs12930834
1 16 72917728 intron variant A/C snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs16972552
rs16972552
1 16 73776555 intron variant C/G;T snv 0.700 1.000 1 2019 2019