Variants in gene RIN2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_018993.4(RIN2):c.1141C>T (p.Arg381Trp)	rs199954296	0.00249
NM_018993.4(RIN2):c.1427C>G (p.Pro476Arg)	rs35142632	0.00165
NM_018993.4(RIN2):c.2501A>T (p.Tyr834Phe)	rs183141566	0.00108
NM_018993.4(RIN2):c.1004C>G (p.Pro335Arg)	rs200780805	0.00098
NM_018993.4(RIN2):c.1045C>T (p.Pro349Ser)	rs201486809	0.00097
NM_018993.4(RIN2):c.2627T>C (p.Ile876Thr)	rs202076384	0.00077
NM_018993.4(RIN2):c.-20G>A	rs375404772	0.00021
NM_018993.4(RIN2):c.404G>A (p.Arg135His)	rs200460217	0.00009
NM_018993.4(RIN2):c.2260G>A (p.Glu754Lys)	rs375974979
NM_018993.4(RIN2):c.77C>T (p.Ser26Leu)	rs577973228

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