C3808988[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1337090	NM_005236.3(ERCC4):c.1853G>A (p.Arg618His)	ERCC4 (R618H)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group Q +5 more	GUncertain significance
Select item 134137	NM_005236.3(ERCC4):c.2545C>G (p.Gln849Glu)	ERCC4 (Q849E)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group Q +5 more	GConflicting classifications of pathogenicity