ClinVar Miner

Submissions for variant NM_173086.5(KRT6C):c.816+13A>G

gnomAD frequency: 0.27989  dbSNP: rs7487256
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 RCV001731076 SCV001981176 benign Palmoplantar keratoderma, nonepidermolytic, focal or diffuse 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707698 SCV005229517 benign not provided criteria provided, single submitter not provided

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