ClinVar Miner

Submissions for variant NM_003476.5(CSRP3):c.160_164delinsAGGGG (p.Ser54_Glu55delinsArgGly)

dbSNP: rs281865416
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000009324 SCV000029542 pathogenic Hypertrophic cardiomyopathy 12 2003-03-18 no assertion criteria provided literature only
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000009324 SCV000189495 not provided Hypertrophic cardiomyopathy 12 no assertion provided not provided

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