rs151045328, USH1C

N. diseases: 2
Source: BEFREE ×
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.
USHER SYNDROME, TYPE IC
CUI: C1848604
Disease: USHER SYNDROME, TYPE IC
1 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.720 1.000 2 2002 2017
Blindness
CUI: C0456909
Disease: Blindness
16 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.010 1.000 1 2013 2013