rs180177168, AGXT

N. diseases: 2
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.
Primary hyperoxaluria, type I
CUI: C0268164
Disease: Primary hyperoxaluria, type I
169 0.925 0.160 2 240868987 missense variant G/A;C;T snv 4.0E-06 0.800 1.000 10 1999 2012
Hyperoxaluria
CUI: C0020500
Disease: Hyperoxaluria
3 0.925 0.160 2 240868987 missense variant G/A;C;T snv 4.0E-06 0.010 1.000 1 2010 2010