rs768965053, NOTCH3

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.
CADASIL Syndrome
CUI: C0751587
Disease: CADASIL Syndrome
23 1.000 0.160 19 15192398 missense variant G/A;T snv 2.4E-05; 4.0E-06 0.010 1.000 1 2012 2012