ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.207+37A>G

dbSNP: rs2272105
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251237 SCV000316208 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001722358 SCV001949280 benign not provided 2018-11-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316455 SCV004015555 likely benign Legius syndrome 2023-07-07 criteria provided, single submitter clinical testing

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