ClinVar Miner

Submissions for variant NM_004744.5(LRAT):c.*2258_*2259insTGTTGTGCTGAGTTT

dbSNP: rs372786858
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000347036 SCV000447959 likely benign Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000384722 SCV000447960 likely benign Retinal dystrophy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000288526 SCV000447961 likely benign Retinitis Pigmentosa, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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