rs12456492, RIT2

N. diseases: 3
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.080 18 43093415 intron variant A/G snv 0.33 0.890 0.909 11 2012 2020
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.882 0.080 18 43093415 intron variant A/G snv 0.33 0.010 1.000 1 2017 2017
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.882 0.080 18 43093415 intron variant A/G snv 0.33 0.010 1.000 1 2017 2017