rs797045014, NOTCH3

N. diseases: 4
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.
CADASIL Syndrome
CUI: C0751587
Disease: CADASIL Syndrome
23 0.851 0.160 19 15192182 missense variant G/A;T snv 0.710 1.000 2 1997 2000
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
CUI: C4551768
Disease: CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
44 0.851 0.160 19 15192182 missense variant G/A;T snv 0.700 1.000 2 2010 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.851 0.160 19 15192182 missense variant G/A;T snv 0.700 0
Transient Cerebral Ischemia
CUI: C0917805
Disease: Transient Cerebral Ischemia
9 0.851 0.160 19 15192182 missense variant G/A;T snv 0.700 0