ClinVar Miner

List of variants in gene CRB1 reported as benign for Leber congenital amaurosis

Included ClinVar conditions (39):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_201253.3(CRB1):c.*28T>C rs41302107
NM_201253.3(CRB1):c.1410= (p.Leu470=) rs3902057
NM_201253.3(CRB1):c.2128+15A>C rs75691013
NM_201253.3(CRB1):c.2306G>A (p.Arg769His) rs62636287
NM_201253.3(CRB1):c.2677-8C>T rs73071678
NM_201253.3(CRB1):c.71-12A>T rs12042179
NM_201253.3(CRB1):c.99G>T (p.Arg33Ser) rs59691602

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