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: rs876657633
rs876657633
1 1.000 0.120 16 2300001 splice donor variant GCACCTT/TGG delins 0.700 1.000 2 2008 2014