ClinVar Miner

Submissions for variant NM_170606.3(KMT2C):c.7846C>T (p.Pro2616Ser)

gnomAD frequency: 0.00010  dbSNP: rs142938767
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
Invitae RCV003727618 SCV004534024 benign not provided 2024-01-17 criteria provided, single submitter clinical testing
ITMI RCV000121488 SCV000085682 not provided not specified 2013-09-19 no assertion provided reference population

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