List of variants in gene QRICH1 reported as likely pathogenic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_198880.3(QRICH1):c.1304A>G (p.Gln435Arg)	rs2106903188
NM_198880.3(QRICH1):c.1649A>G (p.Tyr550Cys)	rs2106862882
NM_198880.3(QRICH1):c.2266C>T (p.Arg756Trp)	rs757870894
NM_198880.3(QRICH1):c.651dup (p.Ala218fs)	rs2106906092

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