List of variants in gene ERCC6L2 reported as likely benign for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020207.7(ERCC6L2):c.3480T>C (p.Val1160=)	rs150957564	0.00078
NM_020207.7(ERCC6L2):c.3839A>C (p.Gln1280Pro)	rs554013810	0.00001

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