List of variants reported as uncertain significance for cataract 9 multiple types by Labcorp Genetics (formerly Invitae), Labcorp

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000394.4(CRYAA):c.335G>A (p.Arg112His)	rs200594555	0.00008
NM_000394.4(CRYAA):c.355C>T (p.Arg119Cys)	rs369609046	0.00008
NM_000394.4(CRYAA):c.202C>T (p.Arg68Trp)	rs376164744	0.00006
NM_000394.4(CRYAA):c.464C>A (p.Ala155Asp)	rs143992484	0.00003
NM_000394.4(CRYAA):c.75G>C (p.Gln25His)	rs754701447	0.00002
NM_000394.4(CRYAA):c.508G>A (p.Ala170Thr)	rs1227057051	0.00001
NC_000021.8:g.(?_43160998)_(47865240_?)dup
NM_000394.4(CRYAA):c.190-24_190-10del
NM_000394.4(CRYAA):c.199G>C (p.Asp67His)	rs747872625
NM_000394.4(CRYAA):c.318C>A (p.Asp106Glu)
NM_000394.4(CRYAA):c.322_327dup (p.Gly108_Tyr109dup)	rs2146498671
NM_000394.4(CRYAA):c.35G>A (p.Arg12His)	rs776884812
NM_000394.4(CRYAA):c.466G>A (p.Glu156Lys)
NM_000394.4(CRYAA):c.506C>T (p.Ser169Leu)
NM_000394.4(CRYAA):c.50T>C (p.Phe17Ser)
NM_000394.4(CRYAA):c.514T>C (p.Ser172Pro)

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