ClinVar Miner

List of variants in gene CRX studied for Benign concentric annular macular dystrophy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000554.6(CRX):c.449C>G (p.Ser150Ter)	rs864309706
NM_000554.6(CRX):c.660del (p.Tyr221fs)	rs864309707
NM_000554.6(CRX):c.661del (p.Tyr221fs)	rs864309708

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