ClinVar Miner

Submissions for variant NM_000477.7(ALB):c.166C>T (p.Gln56Ter)

dbSNP: rs75470261
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000144398 SCV000189453 not provided Analbuminemia no assertion provided not provided
OMIM RCV000144398 SCV001683258 pathogenic Analbuminemia 1994-03-15 no assertion criteria provided literature only

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