rs9975788, MIR99AHG

N. diseases: 1
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.
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 21 16092495 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012