List of variants in gene EXT2 reported as likely pathogenic for not provided

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_207122.2(EXT2):c.1945C>T (p.Arg649Ter)	rs765648513	0.00004
NM_207122.2(EXT2):c.1305+2T>C	rs202153611	0.00001
NM_207122.2(EXT2):c.1179dup (p.Trp394fs)	rs1955074882
NM_207122.2(EXT2):c.1778del (p.Val593fs)
NM_207122.2(EXT2):c.553_558del (p.Asn185_His186del)	rs761364688
NM_207122.2(EXT2):c.626+1G>T	rs1057521132
NM_207122.2(EXT2):c.93del (p.Ile32fs)

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