Variants in gene EXT2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
NM_207122.2(EXT2):c.710C>T (p.Ser237Leu)	rs139525250	0.00236
NM_207122.2(EXT2):c.1588G>A (p.Glu530Lys)	rs148711133	0.00079
NM_207122.2(EXT2):c.1760C>T (p.Thr587Met)	rs138495222	0.00063
NM_207122.2(EXT2):c.1087G>A (p.Val363Met)	rs138943091	0.00046
NM_207122.2(EXT2):c.1022C>T (p.Pro341Leu)	rs141035971	0.00044
NM_207122.2(EXT2):c.1912G>A (p.Val638Ile)	rs145024832	0.00031
NM_207122.2(EXT2):c.260T>G (p.Met87Arg)	rs140075817	0.00031
NM_207122.2(EXT2):c.1645C>T (p.Leu549=)	rs142565472	0.00025
NM_207122.2(EXT2):c.1916C>T (p.Thr639Met)	rs138722406	0.00010
NM_207122.2(EXT2):c.1685G>A (p.Arg562Gln)	rs140561784	0.00008
NM_207122.2(EXT2):c.284G>A (p.Arg95His)	rs143703574	0.00005
NM_207122.2(EXT2):c.383G>A (p.Arg128Gln)	rs771039412	0.00003
NM_207122.2(EXT2):c.11C>T (p.Ser4Leu)	rs527624522	0.00002
NM_207122.2(EXT2):c.198G>C (p.Val66=)	rs775542605
NM_207122.2(EXT2):c.245A>C (p.Asp82Ala)	rs534539796
NM_207122.2(EXT2):c.520A>C (p.Met174Leu)	rs111589746

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