List of variants in gene RIN2 reported as pathogenic for RIN2 syndrome

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.1731del (p.Ile578fs)	rs759390822
NM_018993.4(RIN2):c.1731dup (p.Ile578fs)	rs759390822
NM_018993.4(RIN2):c.1914_1915del (p.Glu638fs)	rs587776915
NM_018993.4(RIN2):c.2104dup (p.Leu702fs)	rs1568718508

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