List of variants in gene HYCC1 reported as uncertain significance by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_032581.4(HYCC1):c.1492A>G (p.Thr498Ala)	rs143894913	0.00403
NM_032581.4(HYCC1):c.766G>C (p.Ala256Pro)	rs142984808	0.00068
NM_032581.4(HYCC1):c.628A>G (p.Ile210Val)	rs372377823	0.00008
NM_032581.4(HYCC1):c.158T>G (p.Leu53Arg)	rs72549407	0.00002
NM_032581.4(HYCC1):c.626+5A>G	rs778280191	0.00002
NM_032581.4(HYCC1):c.896G>A (p.Arg299Lys)	rs142028582	0.00001

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