rs398122917, CLIC2

N. diseases: 5
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.
MENTAL RETARDATION, X-LINKED, SYNDROMIC 32
CUI: C3550913
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC 32
1 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 0.800 1.000 1 2012 2012
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 0.010 1.000 1 2012 2012
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 0.010 1.000 1 2012 2012
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 0.010 1.000 1 2012 2012
Seizures
CUI: C0036572
Disease: Seizures
553 0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 0.010 1.000 1 2012 2012