List of variants in gene RIN2 reported as benign for congenital entropion

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.1818C>T (p.His606=)	rs2076584	0.35224
NM_018993.4(RIN2):c.2201-47G>A	rs6136905	0.10785
NM_018993.4(RIN2):c.85G>A (p.Gly29Arg)	rs78648341	0.01238

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