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: rs865488
rs865488
TG
4 0.882 8 132926377 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019