List of variants reported as likely benign for pigmented paravenous retinochoroidal atrophy by Illumina Laboratory Services, Illumina

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.484G>A (p.Val162Met)	rs137853138	0.00106
NM_201253.3(CRB1):c.3992G>A (p.Arg1331His)	rs62636285	0.00078
NM_201253.3(CRB1):c.1647T>C (p.Asn549=)	rs62636283	0.00064
NM_201253.3(CRB1):c.614T>C (p.Ile205Thr)	rs62645749	0.00049
NM_201253.3(CRB1):c.664G>A (p.Glu222Lys)	rs114846212	0.00014
NM_201253.3(CRB1):c.2714G>A (p.Arg905Gln)	rs114052315	0.00011
NM_201253.3(CRB1):c.2874C>T (p.Ser958=)	rs372778560	0.00003
NM_201253.3(CRB1):c.867G>A (p.Thr289=)	rs147244321	0.00002
NM_201253.3(CRB1):c.265C>T (p.Pro89Ser)	rs145525029	0.00001
NM_201253.3(CRB1):c.2715G>A (p.Arg905=)	rs534108312	0.00001
NM_201253.3(CRB1):c.4005+4AGC[3]	rs550852869

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