Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 115482713
Gene Symbol: H3P10
H3P10
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.020 GeneticVariation BEFREE Recognition of p16 mutations as an etiological factor in familial HNSCC provides an accessible tool for diagnosis of this syndrome. 12461329

2002
Entrez Id: 115482713
Gene Symbol: H3P10
H3P10
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.020 GeneticVariation BEFREE Novel germline p16 mutation in familial malignant melanoma in southern Sweden. 8653684

1996