List of variants in gene EXT1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_000127.3(EXT1):c.1782G>A (p.Ala594=)	rs61753261	0.00058
NM_000127.3(EXT1):c.1503C>T (p.Leu501=)	rs146108006
NM_000127.3(EXT1):c.529A>G (p.Lys177Glu)

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