List of variants in gene HERC2 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004667.6(HERC2):c.10021C>T (p.Gln3341Ter)	rs371406398	0.00024
NC_000015.9:g.(?_28544548)_(28544662_?)dup
NM_004667.6(HERC2):c.11218C>T (p.Arg3740Ter)	rs2548872276
NM_004667.6(HERC2):c.5846-1G>A

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