List of variants in gene CRX reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000554.6(CRX):c.*436G>T	rs759530877	0.01473
NM_000554.6(CRX):c.*727C>T	rs1360823353	0.00103
NM_000554.6(CRX):c.11A>G (p.Tyr4Cys)	rs1211313175	0.00002
NM_000554.6(CRX):c.*435del	rs886054551
NM_000554.6(CRX):c.754_756dup	rs60558029
NM_000554.6(CRX):c.*756dup	rs60558029

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