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: rs7077800
rs7077800
1 10 25530299 intron variant C/T snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs7086249
rs7086249
1 10 25522506 intron variant T/C snv 0.52 0.700 1.000 1 2018 2018