rs1553417206, EXOC6B

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Dysmorphic features
CUI: C0432072
Disease: Dysmorphic features
617 1.000 2 72465341 splice acceptor variant T/C snv 0.700 1.000 1 2016 2016
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 1.000 2 72465341 splice acceptor variant T/C snv 0.700 1.000 1 2016 2016