ClinVar Miner

Submissions for variant NM_012275.3(IL36RN):c.304C>T (p.Arg102Trp)

gnomAD frequency: 0.00001  dbSNP: rs199932303
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001200640 SCV001371649 uncertain significance not provided 2022-05-01 criteria provided, single submitter clinical testing IL36RN: PM2, BP4
Fulgent Genetics, Fulgent Genetics RCV002492539 SCV002781261 uncertain significance Acrodermatitis continua suppurativa of Hallopeau 2022-04-28 criteria provided, single submitter clinical testing
OMIM RCV002492539 SCV000195547 pathogenic Acrodermatitis continua suppurativa of Hallopeau 2013-05-01 no assertion criteria provided literature only

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