"NXF5-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 711146	NR_028089.1(NXF5):n.1420C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	not provided +1 more	GBenign
Select item 2055722	NR_028089.1(NXF5):n.1324G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	NXF5-related condition +1 more	GConflicting classifications of pathogenicity
Select item 1289138	NR_028089.1(NXF5):n.1103G>A	NXF5	Single nucleotide variant (non-coding transcript variant)	not provided +1 more	GBenign
Select item 3032811	NC_000023.11:g.101838414G>A	NXF5	Single nucleotide variant	NXF5-related condition	GLikely benign
Select item 2714827	NC_000023.11:g.101841670A>C	NXF5	Single nucleotide variant	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1600767	NR_028089.1(NXF5):n.427A>G	NXF5	Single nucleotide variant (non-coding transcript variant)	NXF5-related condition +1 more	GBenign
Select item 726012	NR_028089.1(NXF5):n.367C>T	NXF5	Single nucleotide variant (non-coding transcript variant)	NXF5-related condition +1 more	GLikely benign

ClinVar