List of variants in gene DHX38 reported as uncertain significance for retinitis pigmentosa 84

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_014003.4(DHX38):c.55G>A (p.Asp19Asn)	rs145829337	0.00094
NM_014003.4(DHX38):c.923C>T (p.Thr308Met)	rs61749038	0.00051
NM_014003.4(DHX38):c.2065G>T (p.Ala689Ser)	rs1408544161	0.00001
NM_014003.4(DHX38):c.605A>G (p.His202Arg)	rs2144134233
NM_014003.4(DHX38):c.716A>G (p.Tyr239Cys)	rs181471020
NM_014003.4(DHX38):c.995G>A (p.Gly332Asp)	rs587777554

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