rs151045328, USH1C

N. diseases: 5
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.
USHER SYNDROME, TYPE IC
CUI: C1848604
Disease: USHER SYNDROME, TYPE IC
36 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.720 1.000 2 2002 2017
Deafness, Autosomal Recessive 18
CUI: C1865870
Disease: Deafness, Autosomal Recessive 18
38 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.700 1.000 5 2000 2007
Usher Syndrome, Type I
CUI: C1568247
Disease: Usher Syndrome, Type I
168 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.700 1.000 3 2000 2005
Usher Syndrome
CUI: C0271097
Disease: Usher Syndrome
74 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.700 1.000 1 2000 2000
Blindness
CUI: C0456909
Disease: Blindness
34 0.851 0.200 11 17531431 synonymous variant C/T snv 3.6E-05 2.1E-05 0.010 1.000 1 2013 2013