List of variants in gene RIN2 reported as uncertain significance by Gharavi Laboratory, Columbia University

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.-36-2791del	rs1568572045
NM_018993.4(RIN2):c.916_917insGC (p.Ser306fs)	rs1568686983
NM_018993.4(RIN2):c.923dup (p.Pro309fs)	rs1568687023
NM_018993.4(RIN2):c.928_929del (p.Arg310fs)	rs1568687231

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