rs753756017, CDH23

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.
Congenital deafness
CUI: C0339789
Disease: Congenital deafness
11 0.925 0.240 10 71812296 intron variant G/A snv 1.5E-04 5.0E-04 0.010 1.000 1 2016 2016
Retinitis Pigmentosa
CUI: C0035334
Disease: Retinitis Pigmentosa
541 0.925 0.240 10 71812296 intron variant G/A snv 1.5E-04 5.0E-04 0.010 1.000 1 2016 2016