ClinVar Miner

Submissions for variant NM_153490.3(KRT13):c.114C>T (p.Ser38=)

gnomAD frequency: 0.87031  dbSNP: rs8182306
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001731065 SCV001981154 benign White sponge nevus 2 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710344 SCV005249792 benign not provided criteria provided, single submitter not provided

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