ClinVar Miner

Submissions for variant NM_024598.4(USB1):c.693+1G>T

dbSNP: rs1292827495
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 RCV000599560 SCV000700238 not provided Poikiloderma with neutropenia no assertion provided literature only

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