ClinVar Miner

Submissions for variant NM_002016.2(FLG):c.5883C>A (p.His1961Gln)

dbSNP: rs3126079
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001688216 SCV001908533 benign not provided 2020-04-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003339719 SCV004050236 benign Ichthyosis vulgaris 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001688216 SCV005286378 benign not provided criteria provided, single submitter not provided

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