ClinVar Miner

Submissions for variant NM_001481.3(GAS8):c.90+1487_90+1488insGCTGCCCCGCAG

dbSNP: rs1555648296
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
Laboratorio de Genetica Humana; Universidad de los Andes RCV000193263 SCV000249555 likely benign Autism 2013-10-01 no assertion criteria provided research

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