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: rs10788569
rs10788569
2 10 87844975 non coding transcript exon variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs10887759
rs10887759
1 10 87843667 intron variant G/A snv 0.12 0.700 1.000 1 2018 2018