List of variants in gene combination CHM, LOC129391306 reported as uncertain significance for retinal disorder

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.352C>G (p.Leu118Val)	rs1355442853	0.00002
NM_000390.4(CHM):c.368C>T (p.Ala123Val)	rs372532715	0.00002
NM_000390.4(CHM):c.385A>G (p.Asn129Asp)	rs759598256	0.00001

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