ClinVar Miner

Submissions for variant NM_018389.5(SLC35C1):c.923C>G (p.Thr308Arg)

dbSNP: rs28937886
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000005006 SCV000025182 pathogenic Leukocyte adhesion deficiency type II 2002-06-15 no assertion criteria provided literature only

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