rs397514624, COL4A1

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.
HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO
CUI: C3281105
Disease: HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO
2 0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 0.800 1.000 1 2012 2012
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 2012 2012
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 0.010 1.000 1 2012 2012