C4748725[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 858580	NM_014003.4(DHX38):c.55G>A (p.Asp19Asn)	DHX38 (D19N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1399641	NM_014003.4(DHX38):c.605A>G (p.His202Arg)	DHX38 (H202R)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 84 +1 more	GUncertain significance
Select item 840809	NM_014003.4(DHX38):c.923C>T (p.Thr308Met)	DHX38 (T308M)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1170574	NM_014003.4(DHX38):c.1386+17C>T	DHX38	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1013901	NM_014003.4(DHX38):c.2065G>T (p.Ala689Ser)	DHX38 (A689S)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 84 +1 more	GUncertain significance
Select item 842571	NM_014003.4(DHX38):c.2831G>A (p.Arg944Gln)	DHX38, LOC126862391 (R944Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar