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: rs60780116
rs60780116
1 1.000 0.080 4 184787653 intron variant T/C snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs735949
rs735949
1 0.925 0.080 4 184795078 intron variant T/C snv 0.10 0.700 1.000 1 2018 2018