List of variants in gene CRYAA reported as likely pathogenic for cataract

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000394.4(CRYAA):c.34C>T (p.Arg12Cys)	rs397515624
NM_000394.4(CRYAA):c.440del (p.Gln147fs)	rs1114167311
NM_000394.4(CRYAA):c.61C>T (p.Arg21Trp)	rs397515625

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