ClinVar Miner

Submissions for variant NM_003701.4(TNFSF11):c.532+4_532+8del

dbSNP: rs2137905441
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000007388 SCV000027587 pathogenic Autosomal recessive osteopetrosis 2 2007-08-01 no assertion criteria provided literature only

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