ClinVar Miner

List of variants reported as likely pathogenic for Peters plus syndrome by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (1):

Peters plus syndrome

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_194318.4(B3GLCT):c.161-1G>T
NM_194318.4(B3GLCT):c.71-1G>T
NM_194318.4(B3GLCT):c.851-1G>T

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