ClinVar Miner

Submissions for variant NC_000011.10:g.117986053G>T

gnomAD frequency: 0.00093  dbSNP: rs867553241
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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 RCV001511663 SCV001718945 benign Inflammatory bowel disease 28 2022-10-25 criteria provided, single submitter clinical testing

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