ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.102G>T (p.Lys34Asn)

dbSNP: rs1476737505
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine RCV001258210 SCV001435105 uncertain significance Andersen Tawil syndrome criteria provided, single submitter clinical testing

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