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: rs10169613
rs10169613
1 1.000 0.080 2 111177400 intron variant C/T snv 0.42 0.700 1.000 1 2018 2018