"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RTTN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 381801	NM_173630.4(RTTN):c.5745+13G>T	RTTN	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 516678	NM_173630.4(RTTN):c.5319G>C (p.Ala1773=)	RTTN	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to RTTN deficiency +2 more	GBenign/Likely benign
Select item 130183	NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)	RTTN (R1630T +1 more)	Single nucleotide variant (missense variant)	RTTN-related disorder +3 more	GBenign/Likely benign
Select item 130198	NM_173630.4(RTTN):c.805T>C (p.Phe269Leu)	RTTN (F269L)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 386467	NM_173630.4(RTTN):c.220-12T>C	RTTN	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 130175	NM_173630.4(RTTN):c.32-3C>T	RTTN	Single nucleotide variant (intron variant)	not specified +3 more	GBenign/Likely benign

ClinVar