rs10779646, KCNK2

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.
Psychotic symptom
CUI: C0871189
Disease: Psychotic symptom
21 1 215152892 intron variant G/A snv 0.56 0.010 1.000 1 2015 2015