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: rs10905284
rs10905284
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3802597
rs3802597
1 10 8072425 intron variant A/G snv 0.44 0.700 1.000 1 2019 2019