ClinVar Miner

Submissions for variant NM_001270987.2(LTBR):c.39+11C>T (rs72645137)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000401002 SCV000380789 likely benign Cystic Fibrosis-Like Syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000312293 SCV000380790 likely benign Pseudohypoaldosteronism type 1 autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing

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