List of variants in gene RIN2 reported as likely benign for RIN2 syndrome

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.84C>T (p.Ile28=)	rs181853315	0.00670
NM_018993.4(RIN2):c.1851C>T (p.Ala617=)	rs180817901	0.00173
NM_018993.4(RIN2):c.2436C>T (p.Tyr812=)	rs540923982	0.00007
NM_018993.4(RIN2):c.159-17G>A	rs372254069	0.00004
NM_018993.4(RIN2):c.899G>A (p.Gly300Asp)	rs751256990	0.00001
NM_018993.4(RIN2):c.1642G>A (p.Val548Met)	rs181298473

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