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

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.3750-238C>T	rs2146485	0.92533
NM_201253.3(CRB1):c.849-35T>C	rs1337167	0.82735
NM_201253.3(CRB1):c.849-231C>G	rs1337168	0.82523
NM_201253.3(CRB1):c.652+240T>C	rs580067	0.69586
NM_201253.3(CRB1):c.71-144A>G	rs550098	0.68877
NM_201253.3(CRB1):c.71-135T>C	rs12042924	0.40904
NM_201253.3(CRB1):c.4006-92G>T	rs1135810	0.34817
NM_201253.3(CRB1):c.849-62T>G	rs1572514	0.24628
NM_201253.3(CRB1):c.988+155A>G	rs1538037	0.08231
NM_201253.3(CRB1):c.*28T>C	rs41302107	0.07060
NM_201253.3(CRB1):c.848+133A>G	rs78935001	0.03348
NM_201253.3(CRB1):c.1171+116G>A	rs2253346	0.03048
NM_201253.3(CRB1):c.988+35C>T	rs2275251	0.02967
NM_201253.3(CRB1):c.989-111C>G	rs114936900	0.02151
NM_201253.3(CRB1):c.2128+15A>C	rs75691013	0.01643
NM_201253.3(CRB1):c.2677-8C>T	rs73071678	0.00970
NM_201253.3(CRB1):c.2677-129C>A	rs16841475	0.00805
NM_201253.3(CRB1):c.99G>T (p.Arg33Ser)	rs59691602	0.00655
NM_201253.3(CRB1):c.1470C>T (p.Gly490=)	rs35193230	0.00265
NM_201253.3(CRB1):c.2306G>A (p.Arg769His)	rs62636287	0.00208
NM_201253.3(CRB1):c.988+48T>C	rs6662053	0.00171
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.1533C>T (p.Ala511=)	rs142224492	0.00051
NM_201253.3(CRB1):c.1428C>T (p.Thr476=)	rs62636282	0.00025
NM_201253.3(CRB1):c.3171C>T (p.Asn1057=)	rs62636284	0.00010
NM_201253.3(CRB1):c.1305A>T (p.Gly435=)	rs34813822	0.00009
NM_201253.3(CRB1):c.3878+137A>G	rs980371
NM_201253.3(CRB1):c.70+50_70+52del	rs3831282
NM_201253.3(CRB1):c.989-53T>G	rs2786098

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