ClinVar Miner

Submissions for variant NM_015702.3(MMADHC):c.228dup (p.Asn77fs)

dbSNP: rs864309741
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
GeneReviews RCV000203370 SCV000258519 not provided Methylmalonic aciduria and homocystinuria type cblD no assertion provided literature only

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