ClinVar Miner

Submissions for variant NM_000061.3(BTK):c.895-12T>C

dbSNP: rs1926564625
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics, University Medical Centre Ljubljana RCV001197880 SCV001368663 uncertain significance X-linked agammaglobulinemia with growth hormone deficiency 2016-01-01 criteria provided, single submitter clinical testing This variant was classified as: Uncertain significance. The following ACMG criteria were applied in classifying this variant: PM2,PP3. This variant was detected in hemizygous state.

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