List of variants in gene HERC2 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_004667.6(HERC2):c.10021C>T (p.Gln3341Ter)	rs371406398	0.00024
NC_000015.9:g.(?_28475513)_(28475646_?)del
NM_004667.6(HERC2):c.12988C>T (p.Gln4330Ter)
NM_004667.6(HERC2):c.2797_2798del (p.Leu933fs)	rs777452432
NM_004667.6(HERC2):c.637C>T (p.Arg213Ter)	rs2075831472

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