"NHEJ1-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 509440	NM_024782.3(NHEJ1):c.783C>G (p.Val261=)	LOC126806516, NHEJ1	Single nucleotide variant (synonymous variant +1 more)	NHEJ1-related disorder +3 more	GLikely benign
Select item 211594	NM_024782.3(NHEJ1):c.258C>T (p.Asp86=)	NHEJ1	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 435984	NM_024782.3(NHEJ1):c.57A>G (p.Ala19=)	NHEJ1	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GLikely benign

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