ClinVar Miner

Submissions for variant NM_003400.4(XPO1):c.1385-49A>G

gnomAD frequency: 0.00003  dbSNP: rs587778011
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
ITMI RCV000119937 SCV000084067 not provided not specified 2013-09-19 no assertion provided reference population

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