ClinVar Miner

List of variants in gene CRX reported as uncertain significance for Leber congenital amaurosis

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 4

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HGVS	dbSNP
NM_000554.6(CRX):c.1621_1623dup	rs59559801
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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