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: rs11904127
rs11904127
1 2 85257695 intron variant G/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs2043230
rs2043230
1 2 85256227 intron variant A/T snv 0.52 0.700 1.000 1 2018 2018