ClinVar Miner

Submissions for variant NM_194454.3(KRIT1):c.1411+20_1411+24del

dbSNP: rs886038758
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
PreventionGenetics, part of Exact Sciences RCV000253629 SCV000316890 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV002518666 SCV003477226 likely benign Cerebral cavernous malformation 2023-04-21 criteria provided, single submitter clinical testing

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