ClinVar Miner

Submissions for variant NM_000572.3(IL10):c.6C>T (p.His2=)

gnomAD frequency: 0.00001  dbSNP: rs140486772
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001465447 SCV001669433 likely benign Inflammatory bowel disease 2024-01-04 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002070280 SCV002496981 likely benign not provided 2022-02-01 criteria provided, single submitter clinical testing

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