List of variants in gene combination ERCC6, LOC126860933 reported as benign for Cerebrooculofacioskeletal syndrome 1

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000124.4(ERCC6):c.2751C>T (p.Gly917=)	rs2229760	0.31596
NM_000124.4(ERCC6):c.2825C>T (p.Thr942Met)	rs2228525	0.01573
NM_000124.4(ERCC6):c.2875G>T (p.Val959Leu)	rs190863815	0.00075

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