MED17, mediator complex subunit 17, 9440

N. diseases: 25; N. variants: 4
Disease: Cerebellar atrophy ×
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: rs267607232
rs267607232 		0.925 11 93796509 missense variant T/C snv
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		0.010 1.000 1 2010 2010