"Genome-Nilou Lab"[submitter] AND "SLX4"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 262053	NM_032444.4(SLX4):c.4500T>C (p.Asn1500=)	SLX4	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group P +3 more	GBenign
Select item 241685	NM_032444.4(SLX4):c.3963G>A (p.Pro1321=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 262058	NM_032444.4(SLX4):c.753G>A (p.Ala251=)	SLX4	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign

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