rs267607207, LAMB2

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.
NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES
10 0.925 0.240 3 49123216 missense variant G/T snv 2.5E-04 2.7E-04 0.700 1.000 2 2010 2011
Pierson syndrome
CUI: C1836876
Disease: Pierson syndrome
13 0.925 0.240 3 49123216 missense variant G/T snv 2.5E-04 2.7E-04 0.700 1.000 2 2004 2006