ClinVar Miner

List of variants in gene combination ANKRD11, TRAPPC2L reported as likely benign for autism spectrum disorder

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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NM_013275.6(ANKRD11):c.136G>A (p.Asp46Asn) rs144947610
NM_013275.6(ANKRD11):c.5632T>C (p.Ser1878Pro) rs143743958

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