ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.*529_*530del (rs140024416)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000325731 SCV000418192 benign Paroxysmal extreme pain disorder 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000276422 SCV000418194 benign Inherited Erythromelalgia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000331548 SCV000418195 benign Congenital Indifference to Pain 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000385940 SCV000418196 benign Small fiber neuropathy 2016-06-14 criteria provided, single submitter clinical testing

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