ClinVar Miner

Submissions for variant NM_004863.4(SPTLC2):c.*5989dup

dbSNP: rs149453307
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000287123 SCV000389002 likely benign Neuropathy, hereditary sensory and autonomic, type 1C 2016-06-14 criteria provided, single submitter clinical testing

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