List of variants in gene CRYAB reported as uncertain significance by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_001289808.2(CRYAB):c.460G>A (p.Gly154Ser)	rs150516929	0.00088
NM_001289808.2(CRYAB):c.116C>T (p.Pro39Leu)	rs149787233	0.00020
NM_001289808.2(CRYAB):c.368G>A (p.Arg123Gln)	rs782206421	0.00003
NM_001289808.2(CRYAB):c.487C>T (p.Arg163Cys)	rs186242388	0.00002
NM_001289808.2(CRYAB):c.265C>T (p.Leu89Phe)	rs797044515
NM_001289808.2(CRYAB):c.353T>C (p.Phe118Ser)	rs876657766

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