ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.1507+1_1508-1del

gnomAD frequency: 0.00001  dbSNP: rs1553173467
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
Inserm U 954, Faculté de Médecine de Nancy RCV000190385 SCV000243919 not provided not provided no assertion provided not provided

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