ClinVar Miner

Submissions for variant NM_001270987.2(LTBR):c.39+42G>A (rs72645139)

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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 RCV000325265 SCV000380793 likely benign Pseudohypoaldosteronism type 1 autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000363650 SCV000380794 likely benign Cystic Fibrosis-Like Syndrome 2016-06-14 criteria provided, single submitter clinical testing

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