Gene: FANCM ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57697
Gene Symbol: FANCM
FANCM 		0.110 GeneticVariation disease BEFREE As further evidence, we detected two additional NOA-affected case subjects with independent FANCM homozygous nonsense variants, one from Estonia (p.Gln1701<sup>∗</sup>; rs147021911) and another from Portugal (p.Arg1931<sup>∗</sup>; rs144567652). 30075111 2018
Entrez Id: 57697
Gene Symbol: FANCM
FANCM 		0.110 Biomarker disease HPO