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: rs10998018
rs10998018
3 10 68203197 intron variant G/A snv 0.41 0.700 1.000 2 2019 2019
dbSNP: rs7095607
rs7095607
1 10 68197593 intron variant G/A snv 0.42 0.700 1.000 1 2017 2017