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"penetrance": null,
"phenotypes": [],
"transcript": null,
"entity_name": "RNF43",
"entity_type": "gene",
"publications": [],
"confidence_level": "2",
"mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"mode_of_pathogenicity": ""
}
],
"stats": {
"number_of_strs": 0,
"number_of_genes": 17,
"number_of_regions": 0
},
"types": [
{
"name": "GMS Rare Disease",
"slug": "gms-rare-disease",
"description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
},
{
"name": "GMS signed-off",
"slug": "gms-signed-off",
"description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
}
],
"status": "public",
"hash_id": null,
"regions": [],
"version": "1.2",
"disease_group": "",
"version_created": "2020-03-04T11:24:00.030409Z",
"disease_sub_group": "",
"relevant_disorders": [
"R211",
"R209"
],
"signed_off": "2020-03-04"
}