ClinVar Miner

Submissions for variant NM_000572.3(IL10):c.201G>A (p.Lys67=)

dbSNP: rs2102439750
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001434222 SCV001637025 likely benign Inflammatory bowel disease 2023-12-01 criteria provided, single submitter clinical testing

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