List of variants in gene CRB1 reported as likely benign for not provided

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.600A>G (p.Thr200=)	rs77713666	0.00254
NM_201253.3(CRB1):c.2307C>T (p.Arg769=)	rs151104285	0.00143
NM_201253.3(CRB1):c.484G>A (p.Val162Met)	rs137853138	0.00106
NM_201253.3(CRB1):c.2103C>G (p.Pro701=)	rs144436610	0.00104
NM_201253.3(CRB1):c.3992G>A (p.Arg1331His)	rs62636285	0.00078
NM_201253.3(CRB1):c.2230C>A (p.Arg744=)	rs150412614	0.00025
NM_201253.3(CRB1):c.1075T>G (p.Ser359Ala)	rs533227950	0.00007
NM_201253.3(CRB1):c.3534C>T (p.Ile1178=)	rs753331276	0.00005
NM_201253.3(CRB1):c.276G>C (p.Arg92Ser)	rs751678963	0.00001
NM_201253.3(CRB1):c.3150G>A (p.Arg1050=)	rs775734395	0.00001
NM_201253.3(CRB1):c.3241T>C (p.Tyr1081His)	rs2125499868
NM_201253.3(CRB1):c.3552C>T (p.Asn1184=)	rs1571558174
NM_201253.3(CRB1):c.579T>C (p.Asp193=)	rs1382054822
NM_201253.3(CRB1):c.71-4G>T	rs1461641922
NM_201253.3(CRB1):c.71-8C>T	rs1193968246

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