rs12586774, LINC02306

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.
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 14 25660360 intron variant G/T snv 3.5E-02 0.700 1.000 1 2012 2012
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 14 25660360 intron variant G/T snv 3.5E-02 0.700 1.000 1 2012 2012