List of variants in gene HID1 reported as pathogenic for epilepsy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_030630.3(HID1):c.1297C>T (p.Arg433Trp)	rs994473385	0.00001
NM_030630.3(HID1):c.2318dup (p.Val774fs)	rs2039300041
NM_030630.3(HID1):c.560G>A (p.Gly187Asp)	rs2039494684

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