ClinVar Miner

Submissions for variant NM_001365536.1(SCN9A):c.*771_*772dup

gnomAD frequency: 0.07233  dbSNP: rs144515054
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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 RCV000293873 SCV000418180 benign Congenital Indifference to Pain 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000348745 SCV000418181 benign Inherited Erythromelalgia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000403917 SCV000418182 benign Small fiber neuropathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000299664 SCV000418183 benign Paroxysmal extreme pain disorder 2016-06-14 criteria provided, single submitter clinical testing

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