ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.5656G>A (p.Gly1886Arg)

dbSNP: rs886044754
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg RCV000408529 SCV000281933 likely pathogenic Severe early-childhood-onset retinal dystrophy 2016-01-01 criteria provided, single submitter clinical testing

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