List of variants in gene CTU2 reported as likely benign by Ambry Genetics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001012759.3(CTU2):c.635A>G (p.Asn212Ser)	rs532019224	0.00003
NM_001012759.3(CTU2):c.1503G>T (p.Arg501=)
NM_001012759.3(CTU2):c.1508G>A (p.Cys503Tyr)

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