ClinVar Miner

List of variants in gene combination AP3B2, CPEB1 reported as uncertain significance for autism spectrum disorder

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_001278512.2(AP3B2):c.881A>C (p.Lys294Thr) rs200983489

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