List of variants in gene SEMA4A reported as pathogenic for cone-rod dystrophy

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022367.4(SEMA4A):c.1033G>C (p.Asp345His)	rs267607033	0.00001
NM_022367.4(SEMA4A):c.1049T>G (p.Phe350Cys)	rs267607034

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