ClinVar Miner

Submissions for variant NM_001551.3(IGBP1):c.608T>C (p.Ile203Thr)

gnomAD frequency: 0.00391  dbSNP: rs61755732
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
Eurofins Ntd Llc (ga) RCV000594197 SCV000704542 likely benign not specified 2017-01-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000953119 SCV001099670 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000953119 SCV005210581 likely benign not provided criteria provided, single submitter not provided

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