ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.*244_*247dup

dbSNP: rs143461219
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000283356 SCV000418220 benign Congenital Indifference to Pain 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000406754 SCV000418222 benign Inherited Erythromelalgia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000289285 SCV000418223 benign Small fiber neuropathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000352131 SCV000418224 benign Paroxysmal extreme pain disorder 2016-06-14 criteria provided, single submitter clinical testing

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