ClinVar Miner

Submissions for variant NM_007332.3(TRPA1):c.1905+28C>T

dbSNP: rs2120474
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001838958 SCV002098817 benign Familial episodic pain syndrome with predominantly upper body involvement 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713123 SCV005269033 benign not provided criteria provided, single submitter not provided

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