List of variants in gene QRICH2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_001388453.1(QRICH2):c.1289G>A (p.Arg430Gln)
NM_001388453.1(QRICH2):c.4408A>G (p.Lys1470Glu)
NM_001388453.1(QRICH2):c.4868G>A (p.Arg1623His)

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