ClinVar Miner

Submissions for variant NM_006147.4(IRF6):c.667+27C>G

dbSNP: rs2235375
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243201 SCV000311390 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711708 SCV001943033 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730631 SCV001980730 benign Autosomal dominant popliteal pterygium syndrome 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711708 SCV005286896 benign not provided criteria provided, single submitter not provided

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