ClinVar Miner

Submissions for variant NC_000014.9:g.105856013G>T

dbSNP: rs2142904095
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics Facility, Ludwig-Maximilians-Universität München RCV001824248 SCV002073887 likely pathogenic Autosomal recessive agammaglobulinemia 1 2021-12-28 criteria provided, single submitter clinical testing

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