List of variants in gene ERCC6L2 reported as likely benign for inherited aplastic anemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020207.7(ERCC6L2):c.21G>C (p.Gln7His)	rs139286981	0.00453
NM_020207.7(ERCC6L2):c.3480T>C (p.Val1160=)	rs150957564	0.00078
NM_020207.7(ERCC6L2):c.1380G>A (p.Ala460=)	rs201406110	0.00006
NM_020207.7(ERCC6L2):c.3839A>C (p.Gln1280Pro)	rs554013810	0.00001
NM_020207.7(ERCC6L2):c.8C>A (p.Pro3Gln)	rs151308487

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