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: rs12921916
rs12921916
1 16 20395874 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs77924615
rs77924615
7 1.000 0.080 16 20381010 intron variant G/A snv 0.16 0.700 1.000 1 2019 2019