ClinVar Miner

List of variants reported as likely pathogenic for cataract 21 multiple types by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_005360.5(MAF):c.185C>T (p.Thr62Met)	rs727502771
NM_005360.5(MAF):c.905C>T (p.Ala302Val)	rs1481963503
NM_005360.5(MAF):c.916C>G (p.Arg306Gly)	rs1913781557

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