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Results: 10

NameGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review statusChrLocation
(GRCh38)
1.
GDNFMalignant melanomanot providednot classified by submitter537815676
2.
GDNFHirschsprung disease 3GO-ESP:0.00038(C)risk factor
(Jan 25, 2011)
classified by single submitter537815654
3.
GDNFHirschsprung disease 3risk factor
(Jan 25, 2011)
classified by single submitter537815827
4.
GDNFHirschsprung disease 3GO-ESP:0.00108(T)
GMAF:0.00080(T)
risk factor
(Jan 25, 2011)
classified by single submitter537815839
5.
See casesPathogenic/Likely pathogenic
(Aug 12, 2011)
classified by single submitter537016043 - 39383281
6.
GDNFCongenital central hypoventilation, Hirschsprung disease 3, Pheochromocytoma, modifier of
GO-ESP:0.00269(A)
GMAF:0.00100(A)
conflicting data from submitters
(Jan 25, 2011)
classified by multiple submitters537816010
7.
See casesPathogenic/Likely pathogenic
(Aug 12, 2011)
classified by single submitter536374107 - 51103841
8.
See casesPathogenic/Likely pathogenic
(Aug 12, 2011)
classified by single submitter535700480 - 45260029
9.
See casesPathogenic/Likely pathogenic
(Aug 12, 2011)
classified by single submitter526593632 - 50288555
10.
See casesPathogenic/Likely pathogenic
(Aug 12, 2011)
classified by single submitter554839 - 45649861

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