ClinVar Miner

Submissions for variant NM_001562.4(IL18):c.105A>C (p.Ser35=)

gnomAD frequency: 0.27313  dbSNP: rs549908
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
Breakthrough Genomics, Breakthrough Genomics RCV004709018 SCV005231604 benign not provided criteria provided, single submitter not provided
Department of Cardiology, Chinese Academy of Medical Sciences, Fuwai Hospital RCV001003437 SCV001161732 benign Three Vessel Coronary Disease no assertion criteria provided clinical testing

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