ClinVar Miner

Submissions for variant NM_003380.5(VIM):c.15del (p.Val6fs)

dbSNP: rs864309690
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eye Genetics Research Group, Children's Medical Research Institute RCV000203397 SCV000256020 likely pathogenic Developmental cataract 2015-01-09 no assertion criteria provided research
OMIM RCV000488584 SCV000575901 pathogenic Cataract 30 2015-12-23 no assertion criteria provided literature only

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