List of variants in gene combination PYROXD1, RECQL reported as benign for not specified

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_002907.4(RECQL):c.1731T>C (p.Asn577=)	rs6500	0.11188
NM_002907.4(RECQL):c.1899A>G (p.Gln633=)	rs17849408	0.10892
NM_002907.4(RECQL):c.1856A>T (p.Asn619Ile)	rs2137305371

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