List of variants in gene HERC2 reported as likely benign for multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004667.6(HERC2):c.3687C>T (p.Asp1229=)	rs149204675	0.00190
NM_004667.6(HERC2):c.3133C>T (p.Arg1045Cys)	rs117802902	0.00025

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