rs11682175, ACTG1P22

N. diseases: 4
Source: INFERRED ×
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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 5 2014 2019
Child Development Disorders, Pervasive
CUI: C0008074
Disease: Child Development Disorders, Pervasive
0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 1 2017 2017
Duration of sleep
CUI: C0424574
Disease: Duration of sleep
0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 1 2019 2019
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.925 0.040 2 57760458 intron variant T/C snv 0.38 0.700 1.000 1 2018 2018