List of variants in gene RECQL4 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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_004260.4(RECQL4):c.2953G>A (p.Val985Met)	rs200629599	0.00024
NM_004260.4(RECQL4):c.1132-8C>A	rs370660188	0.00010
NM_004260.4(RECQL4):c.2032G>A (p.Val678Met)	rs780282337	0.00001
NM_004260.4(RECQL4):c.2573C>T (p.Thr858Ile)	rs965539808

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