List of variants in gene CRYAA reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000394.4(CRYAA):c.154C>T (p.Leu52Phe)	rs146914780	0.00234
NM_000394.4(CRYAA):c.335G>A (p.Arg112His)	rs200594555	0.00008
NM_000394.4(CRYAA):c.202C>T (p.Arg68Trp)	rs376164744	0.00006
NM_000394.4(CRYAA):c.146G>A (p.Arg49His)	rs754607706
NM_000394.4(CRYAA):c.245C>G (p.Pro82Arg)

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