C4748725[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1167324	NM_014003.4(DHX38):c.147C>G (p.Leu49=)	DHX38	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 84 +2 more	GBenign
Select item 1167325	NM_014003.4(DHX38):c.418C>A (p.Arg140=)	DHX38	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 84 +2 more	GBenign
Select item 1167326	NM_014003.4(DHX38):c.1308T>C (p.Ala436=)	DHX38	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 84 +2 more	GBenign
Select item 1167327	NM_014003.4(DHX38):c.1698G>A (p.Thr566=)	DHX38	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 84 +2 more	GBenign
Select item 1168651	NM_014003.4(DHX38):c.2316C>A (p.Ala772=)	DHX38	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 84 +2 more	GBenign
Select item 1170141	NM_014003.4(DHX38):c.2380-20T>C	DHX38	Single nucleotide variant (intron variant)	Retinitis pigmentosa 84 +1 more	GBenign
Select item 1167005	NM_014003.4(DHX38):c.2487+14T>C	DHX38	Single nucleotide variant (intron variant)	Retinitis pigmentosa 84 +1 more	GBenign

ClinVar