rs569826109, CERKL

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.
Retinitis Pigmentosa 26
CUI: C1842127
Disease: Retinitis Pigmentosa 26
9 1.000 0.080 2 181604002 missense variant G/A;T snv 5.2E-05; 5.2E-05 0.700 1.000 2 2004 2008
Retinal Dystrophies
CUI: C0854723
Disease: Retinal Dystrophies
227 1.000 0.080 2 181604002 missense variant G/A;T snv 5.2E-05; 5.2E-05 0.700 1.000 1 2008 2008