List of variants in gene GCNT2 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_145649.5(GCNT2):c.*1317G>A	rs137926677	0.00716
NM_001491.3(GCNT2):c.761A>G (p.His254Arg)	rs138593604	0.00020
NM_145649.5(GCNT2):c.1038T>C (p.Ile346=)	rs747738500	0.00004
NM_001491.3(GCNT2):c.169_187dup (p.Lys63fs)	rs773702023

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