ClinVar Miner

Submissions for variant NM_001122681.2(SH3BP2):c.81G>T (p.Val27=)

dbSNP: rs745515987
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000378303 SCV000449185 uncertain significance Fibrous dysplasia of jaw 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000378303 SCV005785618 likely benign Fibrous dysplasia of jaw 2024-08-28 criteria provided, single submitter clinical testing

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