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: rs16861827
rs16861827
1 1.000 0.120 1 18351676 intron variant C/T snv 0.12 0.700 1.000 1 2017 2017