List of variants reported as benign for PCARE-related retinopathy by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.1739C>T (p.Thr580Met)	rs10166913	0.16186
NM_001029883.3(PCARE):c.679G>A (p.Glu227Lys)	rs114057537	0.03342
NM_001029883.3(PCARE):c.755C>A (p.Ala252Asp)	rs77003681	0.01424
NM_001029883.3(PCARE):c.2063G>A (p.Cys688Tyr)	rs149601594	0.00556
NM_001029883.3(PCARE):c.3789G>A (p.Leu1263=)	rs199689791	0.00417
NM_001029883.3(PCARE):c.2875G>A (p.Ala959Thr)	rs192350796	0.00140
NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del)	rs138020654

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