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: rs149989682
rs149989682
10 0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 0.700 1.000 16 2005 2014
dbSNP: rs876657633
rs876657633
1 1.000 0.120 16 2300001 splice donor variant GCACCTT/TGG delins 0.700 1.000 2 2008 2014