List of variants in gene ERCC3 reported as benign by Mendelics

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_000122.2(ERCC3):c.1828-36C>T	rs113416031	0.00050
NM_000122.2(ERCC3):c.1828-33C>T	rs745775695	0.00007
NM_000122.2(ERCC3):c.1828-35C>T	rs1444307407	0.00004
NM_000122.2(ERCC3):c.1828-32A>T	rs773954881

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