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Results: 9

NameGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review statusChrLocation
(GRCh38)
1.
MYO7ARetinitis pigmentosa-deafness syndromePathogenic/Likely pathogenic
(Jun 7, 2012)
classified by single submitter1177158426
2.
MYO7Anot specified, not providedGO-ESP:0.00251(T)Benign/Likely benign
(Mar 11, 2014)
classified by multiple submitters1177162903
3.
MYO7ARetinitis pigmentosa-deafness syndromePathogenic/Likely pathogenic
(Nov 13, 2006)
classified by single submitter1177162179 - 77162180
4.
MYO7Anot specified, not providedGO-ESP:0.08745(A)
GMAF:0.15980(A)
Benign/Likely benign
(Mar 11, 2013)
classified by multiple submitters1177161123
5.
MYO7Anot specified, not providedGO-ESP:0.00415(T)
GMAF:0.00140(T)
Benign/Likely benign
(Jan 24, 2013)
classified by multiple submitters1177147791
6.
MYO7AUsher syndrome, type 1BGMAF:0.01470(T)Pathogenic/Likely pathogenic
(Nov 7, 2012)
classified by single submitter1177142783
7.
MYO7AUsher syndrome, type 1B, not specifiedGO-ESP:0.00188(A)
GMAF:0.00140(A)
conflicting data from submitters
(Nov 7, 2012)
classified by multiple submitters1177158332
8.
MYO7AUsher syndrome, type 1BPathogenic/Likely pathogenic
(Nov 7, 2012)
classified by single submitter1177156903
9.
MYO7ARetinitis pigmentosa-deafness syndrome, Usher syndrome, type 1BPathogenic/Likely pathogenic
(Nov 7, 2012)
classified by multiple submitters1177156904

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