Source: ALL
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: rs991014
rs991014
SETBP1
2 18 44859921 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs9912468
rs9912468
PRKCA
3 17 66322239 intron variant G/A;C snv 0.700 1.000 1 2010 2010