Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2833556
rs2833556 		21 31912988 intron variant G/A snv 0.32
CUI: C0684328
Disease: Reasoning
Reasoning 		0.700 1.000 1 2011 2011