List of variants in gene combination FRAS1, LOC126807089 reported as benign for eyelid 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_025074.7(FRAS1):c.11037C>G (p.Pro3679=)	rs4975070	0.42060
NM_025074.7(FRAS1):c.11056C>T (p.Leu3686=)	rs4975139	0.42041

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