List of variants in gene combination CHM, LOC129391306 reported as likely pathogenic for retinal disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000390.4(CHM):c.355C>T (p.Gln119Ter)	rs1930445401
NM_000390.4(CHM):c.386del (p.Asn129fs)
NM_000390.4(CHM):c.436_439del (p.Leu146fs)	rs1930435879
NM_000390.4(CHM):c.453dup (p.Glu152Ter)

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