List of variants in gene EXT2 reported as likely benign 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_207122.2(EXT2):c.1305+254G>C	rs12791572	0.03058
NM_207122.2(EXT2):c.-31+474G>A	rs112082531	0.02206
NM_207122.2(EXT2):c.-30-80A>C	rs75844681	0.01471
NM_207122.2(EXT2):c.-31+657G>A	rs74980806	0.01266
NM_207122.2(EXT2):c.940-203A>G	rs111293320	0.01038
NM_207122.2(EXT2):c.1017T>C (p.Cys339=)	rs11828047	0.00930
NM_207122.2(EXT2):c.1936-179C>T	rs117782883	0.00722
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.260T>G (p.Met87Arg)	rs140075817	0.00031
NM_207122.2(EXT2):c.1496-204_1496-195del
NM_207122.2(EXT2):c.1496-209del
NM_207122.2(EXT2):c.1936-134GT[10]	rs3832748
NM_207122.2(EXT2):c.404T>C (p.Met135Thr)	rs2134967784
NM_207122.2(EXT2):c.519G>C (p.Ala173=)	rs148121594
NM_207122.2(EXT2):c.626+262C>G	rs76685253
NM_207122.2(EXT2):c.940-79A>C

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