List of variants reported as likely benign for Leber congenital amaurosis 8

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.*28T>C	rs41302107	0.07060
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.2306G>A (p.Arg769His)	rs62636287	0.00208
NM_201253.3(CRB1):c.2307C>T (p.Arg769=)	rs151104285	0.00143
NM_201253.3(CRB1):c.2977G>A (p.Glu993Lys)	rs151092557	0.00122
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.1647T>C (p.Asn549=)	rs62636283	0.00064
NM_201253.3(CRB1):c.1533C>T (p.Ala511=)	rs142224492	0.00051
NM_201253.3(CRB1):c.614T>C (p.Ile205Thr)	rs62645749	0.00049
NM_201253.3(CRB1):c.29T>C (p.Leu10Pro)	rs201609001	0.00029
NM_201253.3(CRB1):c.2230C>A (p.Arg744=)	rs150412614	0.00025
NM_201253.3(CRB1):c.866C>T (p.Thr289Met)	rs62636263	0.00025
NM_201253.3(CRB1):c.1986A>G (p.Ser662=)	rs115400822	0.00021
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.3171C>T (p.Asn1057=)	rs62636284	0.00010
NM_201253.3(CRB1):c.1305A>T (p.Gly435=)	rs34813822	0.00009
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.1014C>A (p.Ile338=)	rs771549675	0.00004
NM_201253.3(CRB1):c.1206T>C (p.Ser402=)	rs373229699	0.00001
NM_201253.3(CRB1):c.1995T>C (p.Asn665=)	rs774597710	0.00001
NM_201253.3(CRB1):c.2715G>A (p.Arg905=)	rs534108312	0.00001
NM_201253.3(CRB1):c.2823G>A (p.Pro941=)	rs62645757	0.00001
NM_201253.3(CRB1):c.4074C>T (p.Ile1358=)	rs753097155	0.00001
NM_201253.3(CRB1):c.2843-3dup	rs776525385
NM_201253.3(CRB1):c.4005+4AGC[3]	rs550852869
NM_201253.3(CRB1):c.579T>C (p.Asp193=)	rs1382054822

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