ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.*416dup

dbSNP: rs3834910
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000364317 SCV000418207 benign Small fiber neuropathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000398126 SCV000418208 benign Paroxysmal extreme pain disorder 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000274625 SCV000418211 benign Inherited Erythromelalgia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000329739 SCV000418212 benign Congenital Indifference to Pain 2016-06-14 criteria provided, single submitter clinical testing

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